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Recalls & Warnings

3/13/2020

FDA Finds Problems at 52% of Supplement Manufacturing Sites in U.S. and 42% Abroad

ConsumerLab.com has obtained results of the FDA's inspections in Fiscal Year 2019 (October 1, 2018 - September 30, 2019) of 598 dietary supplement manufacturing facilities in the U.S.

Product Review

Muscle & Workout Supplements Review (Creatine and Branched-chain Amino Acids)

Find the Best Muscle Enhancement Supplements. See Which BCAA and Creatine Supplements Passed CL's Tests & the Top Picks.

Muscle Enhancement Supplements (Creatine and Branched Chain Amino Acids) Reviewed by ConsumerLab.com

Product Review

Melatonin Supplements Review

Find the Best Melatonin Supplements. Trouble Sleeping? See CL's Tests of Melatonin Supplements and Top Picks.

Melatonin Supplements Reviewed by ConsumerLab.com

Product Review

Multivitamin and Multimineral Supplements Review

Find the Best Multivitamin and Prenatal Supplements -- Including Multis for Pets

Multivitamin/Multimineral Supplements Reviewed by ConsumerLab.com

Recalls & Warnings

3/12/2016

FDA Finds Problems at 58% of Supplement Manufacturing Sites in U.S. and Abroad

ConsumerLab.com has obtained results of the FDA's inspections in Fiscal Year 2015 (ending September 30) of 483 dietary supplement manufacturing facilities, showing that most -- 58.2% -- received letters indicating noncompliance with current Good Manufacturing Practices (cGMPs).

Product Review

Ginger Supplements, Chews & Spices Review

Tests Reveal Best and Worst Ginger Supplements & Spices. Poor Quality and Lead Contamination Discovered in Some Products.

Ginger Supplements Reviewed By Consumerlab.com

Product Review

Magnesium Supplements Review (Including Calcium, Boron, and Vitamins D & K)

Find Out What Magnesium Does, Who Needs It, and Our Top Picks Among Supplements

Product Review

Vitamin D Supplements Review (Including Calcium, Magnesium, Boron, and Vitamin K)

Find the Best Vitamin D Supplement with the Right Dose

Product Review

Zinc Supplements and Lozenges Review

Find the Best Zinc Supplements and Lozenges. Have a Cold? See CL's Top Picks Among Zinc Supplements and Lozenges.

Zinc Supplements and Lozenges Reviewed by ConsumerLab.com

Product Review

Fish Oil, Krill Oil, and Algal Oil Omega-3 (DHA & EPA) Supplements Review

Find the Best Fish Oil & Compare to Prescription Omega-3 Drugs. See Our Top Picks Among Fish Oil & Other Omega-3 Supplements for Adults, Children and Pets.

Fish Oil and Other Marine Oil Supplements Reviewed by ConsumerLab.com

Product Review

Vitamin C Supplements Review

Find the Best Vitamin C Supplement. Tests and Reviews of Popular Vitamin C Supplements & CL's Top Picks.

Vitamin C Supplements Tested by ConsumerLab.com

Product Review

Turmeric and Curcumin Supplements and Spices Review

Find the Best Turmeric and Curcumin Supplements & Spices. Big Differences Discovered Among Brands -- Little Curcumin In Some.

Turmeric and Curcumin Supplements and Spices Reviewed by ConsumerLab.com

Product Review

CoQ10 and Ubiquinol Supplements Review

Find the Best CoQ10 and Ubiquinol Supplements and Learn What They Do

CoQ10 and Ubiquinol Supplements Reviewed by ConsumerLab.com

Product Review

Weight Loss Supplements Review (7-Keto DHEA, Forskolin and Stimulant Blend Supplements)

Choose the Best Weight Loss Supplement. Be Careful With Weight Loss Supplements — Few Pass Quality Testing and Safety Review.

Weight Loss Supplements Tested by ConsumerLab.com

Product Review

Alpha Lipoic Acid Supplements Review

Choose the Best Alpha-Lipoic Acid Supplement. Some Alpha-Lipoic Acid Supplements Cost 13 Times As Much As Others -- But Is It Worth Paying More?

Alpha-Lipoic Acid Supplements Reviewed by ConsumerLab.com

Product Review

B Vitamin Supplements Review (B Complexes, B6, B12, Biotin, Folate, Niacin, Riboflavin & More)

See Which B Vitamins Are ConsumerLab's Top Picks!

Review of B Vitamin Supplements

Product Review

Joint Health Supplements Review (Glucosamine, Chondroitin, MSM, Boswellia, Collagen and Turmeric)

One-Third of Joint Health Supplements Failed to Pass Our Tests. See Which Passed or Failed, and our Top Picks.

Review of Supplements for Joint Pain

Product Review

Vision Supplements Review (with Lutein and Zeaxanthin)

Find the Best Vision Supplement. Tests and Reviews of Popular Vision Supplements.

Lutein, Zeaxanthin and Vision Supplements Tested by ConsumerLab.com

Product Review

Vitamin E Supplements Review

Find the Best Vitamin E Supplement. Tests and Reviews of Popular Vitamin E Supplements & CL's Top Picks.

Vitamin E Supplements, Cream, and Oil Tested by ConsumerLab.com

Product Review

Apple Cider Vinegar Review – Bottled Liquids and Supplements

Find the Best Apple Cider Vinegar. See Which Apple Cider Vinegar Liquids and Supplements Passed Our Tests of Quality.

Apple Cider Vinegar Supplements Reviewed by ConsumerLab.com

Product Review

Protein Powders and Shakes Review

Find Out Which Protein Powders Passed or Failed Our Tests

Product Review

Red Yeast Rice Supplements Review

50% of Red Yeast Rice Supplements "NOT APPROVED" in CL Tests

Product Review

Green Tea Review: Tea Bags, Loose Tea, Matcha Powders, and Supplements

Disturbing Findings for Some Major Brands of Green Tea. See the Test Results and Our Top Picks for Green Tea.

Green Tea Review By ConsumerLab.com

Product Review

Black Currant Oil, Borage Oil, Evening Primrose Oil, Flaxseed Oil, and Hemp Oil Supplements Review: Sources of ALA and GLA (Omega-3 and -6 Fatty Acids)

Choose the Best Seed Oil Supplements. Find Out Which Flaxseed and Other Seed Oil Supplements Passed Our Tests.

Flaxseed Oil, Evening Primrose Oil, Borage Oil, Hemp Oil and Black Currant Oil Supplements Reviewed by ConsumerLab.com

Product Review

Probiotic Supplements Review (Including Pet Probiotics)

Probiotics: See What They Really Contain and Our Top Picks

Product Review

Collagen Supplements Review

The Best Collagen Supplements for Wrinkles and Joints Revealed. Find Out If Collagen Really Works and Which Reviewed Products Are Best In Our Tests and Comparisons.

Collagen Supplements Reviewed By ConsumerLab

Product Review

Calcium and Bone Health Supplements Review (Including Vitamins D & K, Magnesium and Boron)

See Which Bone Health Supplements Are Top Picks and Which Fail

Product Review

Ginseng Supplements Review

Find the Best Ginseng Supplement. Key "Ginsenosides" Found to Range 10-Fold Across Products.

Ginseng Supplements Reviewed by ConsumerLab

Product Review

Ashwagandha Supplements Review

Find the Best Ashwagandha Supplement. Only 56% of Ashwagandha Products Pass Tests.

Ashwagandha supplements reviewed by ConsumerLab.com

Product Review

Menopause Supplements Review (Soy and Red Clover Isoflavones, Black Cohosh) and Progesterone Creams

Choose the Best Menopause Supplement. Find Out Now Which Soy Isoflavone, Red Clover, Black Cohosh, and Progesterone Products Have the Active Compounds You Want!

Menopause Supplements Tested by ConsumerLab.com -- Soy and Red Clover Isoflavones, Black Cohosh, and Progesterone Cream

Product Review

Tuna, Salmon, Sardines & Herring Review (Canned and Packaged)

Find the Best Tuna, Salmon, Sardines & Herring. Avoid Mercury and Arsenic and Maximize EPA & DHA Omega-3s!

Canned tuna, salmon and sardines reviewed by ConsumerLab.com

Product Review

Iron Supplements Review (Iron Pills, Liquids and Chews)

See Which Iron Supplements Are CL's Top Picks for Different Needs

Product Review

CBD & Hemp Extract Supplements, Lotions, and Balms Review

Find the Best CBD at the Lowest Price! Learn How Much CBD (and THC) Is Really in Products and Which Are Our Top Picks.

CBD and Hemp Oils Reviewed by ConsumerLab.com

Product Review

Astaxanthin Supplements Review

See Which Astaxanthin Products Passed or Failed CL's Tests

Astaxanthin supplements reviewed by ConsumerLab.com

Product Review

Lysine Supplements Review

Choose the Best Lysine Supplement. CL Tests Reveal Which Lysine Supplements Provide the Best Quality and Value.

Product Review

Choline and Lecithin Supplements Review (Including Phosphatidylcholine, CDP-Choline, and Alpha-GPC)

Product Review

Resveratrol Supplements Review (From Red Wine, Knotweed, and Other Sources)

See Which Resveratrol Supplements Were Best In Our Tests and Comparisons. Learn What Resveratrol Can and Can't Do.

Review of resveratrol supplements tested by ConsumerLab.com, including ratings and comparisons of product quality, price, and ingredients.

Product Review

Potassium Supplements Review

Be Careful with Potassium Supplements! Problems Found. Tests and Reviews of Potassium Supplements & CL's Top Picks.

Potassium Supplements reviewed by ConsumerLab.com

Product Review

Cholesterol-Lowering Supplements Review (Sterols/Stanols and Policosanol)

Find the Best Cholesterol-Lowering Supplement. See Which Plant Sterol and Policosanol Supplements Passed Our Tests and Are Our Top Picks.

Sterol, Stanol, and Policosanol Supplements for Cholesterol-lowering Reviewed by ConsumerLab.com

Product Review

Whole, Ground, and Milled Flaxseed Review

Caution: High Levels of Cadmium Found In Flaxseed Products

Product Review

Ginkgo (Ginkgo Biloba) Supplements Review

Choose the Best Ginkgo Biloba Supplement. Finding Real Ginkgo Isn't Easy — 60% Fail ConsumerLab's Tests of Quality.

Ginkgo Biloba Supplements Tested by ConsumerLab.com

Product Review

Cinnamon Supplements and Spices Review

CAUTION: Some Cinnamon Products High in Toxin. See Which Passed or Failed and our Top Picks! .

Cinnamon Supplements and Spices Tested by ConsumerLab.com

Product Review

Selenium Supplements Review

Choose the Best Selenium Supplement. Find Out If You Need Selenium and Which Supplement Is Our Top Pick.

Selenium Supplements Reviewed by ConsumerLab.com

Product Review

Alginate Supplements Review (For Reflux)

See Our Top Pick Alginate Supplements For Reducing Symptoms of Gastroesophageal Reflux (GERD)

Alginate supplements reviewed by ConsumerLab.com

Product Review

Elderberry Supplements Review

Find the Best Elderberry Supplement. Tests and Reviews of Popular Elderberry Supplements & CL's Top Picks.

Elderberry Supplements Reviewed by ConsumerLab.com

Product Review

Garlic Supplements Review

Find the Best Garlic Supplements. CL Tests Reveal Big Differences in Garlic Strength -- Some Have Little to No Garlic!.

Garlic Supplements Reviewed by ConsumerLab.com

Product Review

Acai Berry Supplements and Beverages Review

Find the Best Acia Berry Supplements and Beverages. See Which Acai Berry Supplements and Beverages Passed Our Tests of Quality.

Acai berry supplements and beverages reviewed by ConsumerLab.com

Product Review

Lactose Intolerance Products Review (Lactase Enzyme Supplements and Lactose-Free Milks)

Choose the Best Lactase Enzyme Supplement and Lactose-Free Milk. Find a CL Approved Lactose Intolerance Product.

Lactase Supplements Reviewed by ConsumerLab.com

Product Review

Dark Chocolates, Cocoa & Cacao Powders, Nibs, and Supplements Review -- Sources of Flavanols

Is Your Chocolate or Cocoa Healthful or Toxic? Find the Best Dark Chocolate, Cocoa Powder and Cocoa Supplements Based On Our Tests.

Product Review

Bilberry Supplements Review

Choose the Best Bilberry Supplement. Some Bilberry Is Not Authentic!

Bilberry Supplements Reviewed by ConsumerLab.com

Product Review

Nattokinase Supplements Review

Choose the Best Nattokinase Supplement. CL Tests Reveal Which Nattokinase Suppplements Provide the Best Quality & Value.

Nattokinase Supplements Tested by Consumerlab.com

Product Review

Prostate Supplements Review (Saw Palmetto and Beta-Sitosterol)

Find the Best Prostate Supplement for Symptoms of BPH. See Which Prostate Supplement Passed or Failed CL's Tests of Quality.

Product Review

Joint Health Supplements for Pets Review (Glucosamine, Chondroitin, MSM & Boswellia)

See Which Pet Supplements for Joint Health Passed Our Tests and Which Didn't!

Joint Health Supplements for Pets

Product Review

Extra Virgin Olive Oil Review

Most Failed to Be Approved. Find the Best Extra Virgin Olive Oil and Avoid Problems.

Extra virgin olive oils reviewed by ConsumerLab.com

Product Review

Nutrition Bars & Cookies Review (For Energy, Fiber, Protein, Meal Replacement, and Whole Foods)

Find the Best Nutrition Bar or Cookie. ConsumerLab Tests Reveals Not All Nutrition Bars and Cookies Contain What They Claim.

Nutrition Bars Reviewed by ConsumerLab.com (Energy, Fiber, Meal Replacement, Protein, and Whole Food Bars)

Product Review

Garcinia Cambogia (HCA) Supplements Review

Find the Best Garcinia Cambogia Supplement. Choose Carefully! Most Garcinia (HCA) Weight Loss Supplements Lack Listed Amount of Ingredient .

Garcinia Cambogia (HCA) Supplements Reviewed by ConsumerLab.com

Product Review

Electrolytes & Sports Drinks Review

See Which Sports Drinks, Powders, and Pills Deliver the Right Electrolytes

Product Review

Vitamin K Supplements Review (Including Calcium, Magnesium, Boron, and Vitamin D)

Should You Take Vitamin K? Beware of Products That Don't Deliver.

Product Review

Boron Supplements Review (Including Calcium, Magnesium, and Vitamins D & K)

Is Boron Needed for Bone Health? Find Out and See Our Top Pick Among Supplements

Product Review

Green Coffee Bean Extract Supplements Review (for Weight Loss)

Choose the Best Green Coffee Bean Extract. 50% of Green Coffee Bean Extract Supplements Don't Deliver Expected Ingredients.

Green Coffee Bean Extract Supplements Reviewed by ConsumerLab.com

Product Review

L-Theanine Supplements Review

Find the Best L-Theanine Supplement. Find Out If L-Theanine Helps for Stress and Which Products Are Best.

L-Theanine Supplements reviewed by ConsumerLab.com

Product Review

Oat Cereals Review

Find the Best Oatmeal, Oat Bran, Steel Cut Oats, & Cold Cereals. Popular Oat Cereals Tested -- Beware of Unexpected Gluten.

Oat Cereals Tested by ConsumerLab.com

Product Review

L-Arginine Supplements Review

Choose the Best L-Arginine Supplement. Find Out Which L-Arginine Supplement Passed CL's Tests.

L-Arginine Supplements Reviewed by ConsumerLab.com

Product Review

Cranberry Juices and Supplements Review

CL's Tests Show Which Cranberry Juices and Supplements Are Best and Cost the Least

Product Review

Echinacea Supplements Review

Many Echinacea Supplements Fail CL's Tests. Make Sure You Know What You're Getting!

Echinacea supplements reviewed by ConsumerLab.com

Product Review

Fruits, Veggies, and Other Greens Supplements Review (Including Spirulina and Chlorella)

Fruit and Veggie Supplements -- Find Out If They Are Worthwhile and See Our Test Findings

Product Review

Lion's Mane and Chaga Supplements Review

Read Labels Carefully -- Many Can Mislead

Lion's Mane and Chaga Supplements tested by ConsumerLab.com

Product Review

Digestive Enzyme Supplements Review

Big Differences in Strength Found Among Digestive Enzyme Supplements. CL Tests Reveal Which Are Best.

Product Review

Milk Thistle Supplements Review

Find the Best Milk Thistle Supplement. Tests and Reviews of Popular Milk Thistle Supplements & CL's Top Picks.

Milk Thistle and Liver Formula Supplements Reviewed by ConsumerLab.com

Product Review

NAC (N-Acetyl Cysteine) Supplements Review

Choose the Best N-Acetyl Cysteine Supplement. See Our Tests of Popular NAC Supplements and Top Picks for Quality and Value.

N-acetyl cysteine (NAC) supplements tested by ConsumerLab.com

Product Review

Coconut Waters Review

Best Coconut Water? See Our Tests and Comparisons of Popular Brands Looking at Sugar, Electrolytes, Taste and Price.

Coconut Waters Reviewed by ConsumerLab.com

Product Review

Kelp Supplements Review

Choose the Best Kelp Supplement. Be Cautious With Kelp! Only 50% of Supplements Pass CL's Review.

Kelp Supplements Reviewed by ConsumerLab.com

CL Answer

Is it true that protein can strain the kidneys as you get older?

Find out if protein strains the kidneys as you get older, how much protein older adults need and the best way to take protein supplements.

Product Review

Plant-Based Milks Review (Almond, Cashew, Coconut, Flax, Hemp, Macadamia, Oat, Pea, and Soy)

Find the Best Non-Dairy Milk Alternative. ConsumerLab Tests Reveal What's Really In Plant-Based Milks.

Plant Based Milks reviewed by ConsumerLab.com

Product Review

Seaweed Snacks and Foods Review

Tests Reveal Seaweed Snack Risks

Product Review

NAD Booster Supplements Review (NAD+/NADH, Nicotinamide Riboside, and NMN)

How Important Is Boosting NAD+ Levels? Find Out and Learn How Booster Supplements Compare.

NAD Boosters (NAD+/NADH, Nicotinamide Ribose, and NMN)

Product Review

DHEA Supplements Review

Choose the Best DHEA Supplement. Beware of Big Differences in Dose and Price.

DHEA Supplements Tested by ConsumerLab.com

Product Review

PQQ (Pyrroloquinoline Quinone) Supplements Review

Learn What PQQ Does and Which PQQ Supplements are Best

CL Answer

Immunocal is much more expensive than other whey protein isolates - is it worth the extra cost?

Find out how Immunocal, from Immunotec, compares to other whey protein isolates and understand it's costs.

Immunocal: A better whey protein? -- box of Immunocal

CL Answer

Which is the best mask to prevent COVID-19 and how do cloth, disposable, N95, and KN95 masks compare? How can I stop glasses from fogging?

See our Top Picks for masks. Learn how to make COVID-19 masks from materials at home that can be almost as effective as surgical mask and N-95 masks.

Four masks shown for comparison

Product Review

SAMe (S-adenosyl-methionine) Supplements Review

Choose the Best SAMe Supplement. CL Tests Reveal Big Differences in Quality and Cost.

Sam-e supplements reviewed by ConsumerLab.com

Product Review

Rhodiola Rosea Supplements Review

Do Rhodiola Supplements Help With Depression and Anxiety? Find Out and See Which Rhodiola Supplements Provide the Best Quality & Value.

Rhodiola Supplements Reviewed by ConsumerLab.com

Product Review

Sexual Enhancer Supplements Review (with Yohimbe, Horny Goat Weed, Arginine)

Choose the Best Sexual Enhancer Supplement. Only 30% of Selected Sexual Enhancement Supplements Pass Quality Tests.

Product Review

Maca Supplements Review

Choose the Best Maca Supplement. Make Sure Your Maca Supplement Isn't Contaminated With Lead.

Maca Supplements Reviewed by ConsumerLab.com

Product Review

Berberine and Goldenseal Supplements Review

Choose the Best Berberine & Goldenseal Supplements. CL Tests Reveal Problems With 25% of Berberine and 67% of Goldenseal Supplements.

Berberine and goldenseal supplements reviewed by ConsumerLab.com

Product Review

Prebiotic Supplements Review

You Can't Tell How Much Fiber Is Really In Most Prebiotics Without Testing

Product Review

Bone Broth Review

Find the Best Bone Broth. Find Out How Much Collagen and Sodium Is Really In Popular Bone Broths.

Bone Broth Supplements Reviewed by Consumerlab.com

Product Review

Vitamin A Supplements Review, Including Beta-Carotene and Cod Liver Oil

Find the Best Vitamin A Supplement. Best Quality Vitamin A Supplements Identified, Including Cod Liver Oil.

Vitamin A Supplements (Including Cod Liver Oil) Reviewed by ConsumerLab.com

Product Review

Taurine Supplements Review for People, Dogs, and Cats

Find the Best Taurine Supplements. Learn When to Use Taurine and Which Supplement is Best.

Taurine Supplements Reviewed by ConsumerLab.com

Product Review

Lycopene Supplements Review

Find the Best Lycopene Supplements. CL Tests Reveal That Not All Lycopene Supplements Contain What They Claim.

Lycopene Supplements Reviewed by ConsumerLab.com

Product Review

Chromium Supplements Review

Chromium Supplements Review. Best Chromium Supplements Identified -- By Strength.

Chromium Supplements Reviewed by ConsumerLab.com

Product Review

Chia Seed Review – Whole, Ground, and Sprouted Seed, Seed Flour, & Supplements

Find the Best Chia Seeds, Sprouted Chia Powder, Flour, and Chia Supplements. Tests and Reviews of Chia Seeds & CL's Top Picks.

Chia supplements reviewed by ConsumerLab.com

Product Review

Quercetin Supplements Review

Find the Best Quercetin Supplements. ConsumerLab Tests Reveal Not All Quercetin Supplements Contain What They Claim.

Quercetin Supplement Reviewed By ConsumerLab.com

Product Review

Avocado Oil Review

Find the Best Avocado Oil for Purity, Freshness and Taste. Some Others May Include Rotten Avocado or Other Oils.

Avocado oil reviewed by ConsumerLab.com

Product Review

GABA Supplements Review

Does GABA Work As a Supplement?

Product Review

Olive Leaf Extract Supplements Review

Learn What Olive Leaf Does and the Best Brands

Product Review

Aloe Juices, Gels, and Supplements Review

How Much Aloe is Really in Aloe Products? Find Out and See Our Top Picks.

Product Review

CLA (Conjugated Linoleic Acid) Supplements Review (for Slimming)

Choose the Best CLA Supplement. Not All CLA Supplements Contain What You Expect.

CLA Supplements Reviewed by ConsumerLab.com

CL Answer

Does AZO Bladder Control really work for overactive bladder?

AZO Bladder Control information, including results from clinical studies on bladder control, dosage, and safety.

Product Review

Acetyl-L-Carnitine Supplements Review

Choose the Best Acetyl-L-Carnitine Supplement. Don't Overpay! CL Identifies Quality Acetyl-L-Carnitine Supplements at the Best Value.

Acetyl-L-Carnitine Supplements Tested by ConsumerLab.com

Product Review

Low-Dose Lithium Supplements Review

Choose the Best Low-Dose Lithium Supplement. CL Tests Reveal Which Low-Dose Lithium Supplements Offer the Best Quality and Value.

Very Low Lithium Supplements Reviewed by ConsumerLab.com

Product Review

St. John's Wort Supplements Review

Find the Best St. John's Wort Supplement. Only 40% of St. John's Wort Supplements Pass Tests & Strength Varies Widely.

St John's Wort Supplements Reviewed By Consumerlab.com

Product Review

Wellbutrin vs. Generic Bupropion Review

Generic Bupropion Is Not Always The Same As Name-Brand Wellbutrin. CL Tests Reveal Differences Between Generic Bupropion and Name-Brand Wellbutrin.

Product Review

Lavender and Tea Tree Essential Oils Review

Oils Tested for Authenticity and Purity

Recalls & Warnings

9/01/2022

Elite One Source Nutritional Services Warned for Manufacturing, Labeling Violations

On August 5, 2022, the FDA issued a warning letter to dietary supplement manufacturer Nutritional Laboratories International, Inc. (DBA Elite One Source Nutritional Services, Inc.

CL Answer

Does Alpha Brain really improve memory, focus and cognition?

Find out if Alpha Brain really improves memory, focus and cognition. See the clinical evidence and get details about Alpha Brain ingredients, as well as potential side effects and drug interactions. ConsumerLab.com's answer explains.

Does-Alpha-Brain-Work?

Product Review

Meal Replacement & Weight Management Powders and Shakes Review

Find the Best Meal Replacement and Weight Management Products. Only 64% of Meal Powders & Shakes Pass ConsumerLab.com's Tests of Quality.

Meal Replacement Supplements Reviewed by ConsumerLab.com

Product Review

Coconut Oil and Medium Chain Triglycerides (MCT) Oil Review – Semi-Solid and Liquid Oils & Supplements

Find the Best Coconut Oil and MCT Oil. See How These Oils Compare on Medium Chain Triglycerides (MCTs), Quality, and Value.

Coconut and MCT Oils Reviewed by ConsumerLab.com

News Release

6/30/2022

Best Protein Shakes & Drinks According to ConsumerLab Tests. Lead, Excess Sodium Found in Some

  White Plains, New York, June 30, 2022 — Consumers may get more sodium, fat, calories, or even lead, than they bargained for from some protein supplements, according to recent ConsumerLab tests of over 20 popular protein powders and shakes.

CL Answer

Do any supplements help with COVID-19? Do supplements like vitamin D, zinc, vitamin C, or herbals work?

Find out if natural remedies & supplements for coronavirus such as zinc, vitamin C, garlic, or elderberry help to prevent or treat COVID-19.

Supplements for Coronavirus (COVID-19)? -- mask and pills

Recalls & Warnings

9/10/2021

FDA Warns Ten Sellers of "Diabetes" Supplements

On September 7, 2021, the FDA issued warning letters to 10 supplement companies that made drug claims by promoting products to treat diabetes and/or lower blood sugar. Five of the products were sold on Amazon as well as on company websites. The products were promoted with statements such as

CL Answer

What are phytoceramides? Do phytoceramide supplements really work to improve aging skin?

Phytoceramide supplement information, including what they are, what they claim to do, and if they have anti-aging effects.

Phytoceramides for Aging Skin? -- woman looking at skin up close in mirror

CL Answer

What are the health benefits of coconut oil and medium chain triglycerides, such as those used in Bulletproof Coffee?

Learn the health benefits of coconut oil and medium chain triglycerides (MCTs), including evidence from Bulletproof Coffee, clinical studies on obesity, skin, and Alzheimer's disease.

Coconut Oil & MCTs -- Coconuts and coconut oil with coffee cup

News Release

2/25/2022

Top-rated Vitamin and Supplement Brands and Merchants for 2022 Based on Consumer Satisfaction

White Plains, New York, February 25, 2022 — Each year, ConsumerLab.com surveys its free e-newsletter subscribers about the vitamins and supplements that they use. The results below are based on 8,049 responses collected in November/December 2021.

Recalls & Warnings

12/29/2022

EarthLab, Inc. Warned for Promoting Curcumin, Elderberry to Treat Pain & Flu

On November 10, 2022, the FDA issued a warning letter to EarthLab, Inc., dba Wise Woman Herbals following inspection of the company’s website which found statements about the company’s products to be drug claims because they suggest the products can prevent or treat disease.

Product Review

Toprol XL vs. Generic Metoprolol Succinate Extended-release (ER) Tablets Review Article

Choose the Best Blood Pressure Medication. Find Out Why Some Generic Blood Pressure Medications Are Not the Same as the Original & May Increase Blood Pressure or Have Other Disturbing Side Effects.

Toprol vs Generic Metoprolol

Product Review

Huperzine A Supplements Review

Choose the Best Huperzine A Supplement. CL Tests Reveal the Best Huperzine A Supplements for Memory.

Huperzine A Supplements Tested by ConsumerLab.com

CL Answer

Do vitamins, minerals and nutritional supplements lose effectiveness with exposure to high temperatures and is it safe to order supplements by mail in the summer?

Are vitamins and supplements susceptible to heat? Find out if mail ordering during the summer is safe.

Heat's Effect on Supplements in the Mail -- Woman receiving a package

Recalls & Warnings

4/17/2021

NS NY Distributor Inc Male Enhancement Products Recalled Due to Undeclared Drugs

On April 8, 2021, NS NY Distributor Inc issued a recall of all lots of Premium Orgazen 7000 and Ginseng Power 5000 male enhancement capsules because FDA analysis found them to contain sildenafil and/or tadalafil.

Recalls & Warnings

3/31/2005

FDA Warns Marketer of "Vitamin O" Product to Cease Unsubstantiated Claims

The U.S. Food and Drug Adminstration (FDA) has sent a Warning Letter (dated February 8, 2005) to Donald L. Smyth, President, R-Garden Inc., and Rose Creek Health Products, Inc. warning that its "Vitamin O" product was, among other things, being marketed with unsubstantiated health claims.

Recalls & Warnings

3/20/2020

Seller of Rejuvenation Pills Settles Charges of Making False Claims

Health Center, Inc. has agreed to halt their allegedly deceptive advertising claims about three "cure-all" health and wellness products that targeted older consumers nationwide after the Federal Trade Commission (FTC) filed a complaint.

Recalls & Warnings

4/28/2020

Ten Multi-Level Marketing Companies Warned for Coronavirus and Deceptive Earnings Claims

On April 24, 2020, the FTC announced that it sent warning letters to ten multi-level marketing companies for selling products such as essential oils and immune system boosters with unsupported claims that they can treat coronavirus (COVID-19) and/or for misrespresenting potential earnings people ...

Recalls & Warnings

4/25/2017

Beware of Products Which Promise to Treat or Cure Cancer, FDA Warns

On April 25, 2017, the FDA warned consumers to be aware of supplements and other products claiming to cure cancer.

Recalls & Warnings

4/25/2022

Some OTC Skin Lighteners Contain Potentially Harmful Ingredient, Warns FDA

On April 19th, 2022, the FDA issued warnings to 12 companies for selling over-the-counter (OTC) skin-lightening products containing hydroquinone.

Recalls & Warnings

6/02/2022

Walmart Inc. Recalls Joint Supplements With Omega-3, Glucosamine & Curcumin

On May 28, 2022, Walmart Inc. issued a voluntary recall of all lots of Artri Ajo King Joint Supplements after FDA laboratory analysis found the presence of undeclared diclofenac.

Recalls & Warnings

5/09/2022

Natural Organics Keto Capsules Recalled Due to Gluten

On March 6, 2022, Natural Organics, Inc. issued a recall of four lots of NaturePlus Keto Living Sugar Control Capsules that were found to contain gluten.

Recalls & Warnings

6/13/2022

Homeopathic Nasal Spray SnoreStop Recalled Due to Microbial Contamination

On June 9, 2022, Green Pharmaceuticals Inc issued a voluntary nationwide recall of one lot of its SnoreStop NasoSpray, a homeopathic nasal spray promoted to reduce snoring, due to the presence of Providencia rettgeri, a bacterium that can cause severe illness in some people.

Recalls & Warnings

7/14/2022

FDA Warns Seller of Unauthorized COVID-19 Tests

On June 30, 2022, the FDA issued a warning letter to W.H.P.M, Inc. for distributing COVID antigen tests without approval, clearance, or authorization from the FDA while claiming to mitigate, prevent, treat, diagnose, or cure COVID-19 in people.

Recalls & Warnings

1/19/2023

Male Sexual Enhancement Supplement Adam’s Secret Found to Contain Prescription Medication

On January 10, 2023, the FDA issued a warning letter to HIS Enterprise Inc dba Adam’s Secret USA, LLC after laboratory analysis found Adam’s Secret Extra Strength 3000 Platinum, Adam’s Secret Extra Strength Blue, Adam’s Secret Extra Strength Purple, Adam's Secret ...

Recalls & Warnings

1/26/2023

FDA Warns Seller of Canary Seed Omega-3

On November 16, 2022, the FDA issued a warning letter to Evimeria El Aztecano, Inc. following review of the company’s Yerbas Finas Leche de Alpiste con Guanabana y Omega-3 product labeling, which found the product contained less magnesium and potassium than claimed on the label.

Recalls & Warnings

8/17/2022

Seller of Moringa Tea and Other Herbal Products Warned for Drug Claims, Manufacturing Violations

On July 29, 2022, the FDA issued a warning letter to Deggeh Foods, Inc.

Recalls & Warnings

7/25/2022

Nature’s Sunshine Protein Powder Recalled

On July 22, 2022, Nature’s Sunshine Products Inc. issued a recall of two AIVIA Whey Protein Powder Herbs meal replacement products due to undeclared milk.

Recalls & Warnings

4/23/2021

FDA Warns 5 Sellers of Unapproved COVID-19 Tests

Between March 18 and April 6, 2021, the FDA issued warning letters to five companies for selling unapproved, adulterated, and misbranded tests for coronavirus (COVID-19).

News Release

2/25/2021

Top-rated Vitamin and Supplement Brands and Merchants for 2021 Based on Consumer Satisfaction -- Results of the ConsumerLab.com Survey of Vitamin & Supplement Users

White Plains, New York, February 25, 2021 — Each year, ConsumerLab.com surveys its free e-newsletter subscribers about the vitamins and supplements that they use. The results below are based on 9,647 responses collected in November 2020.

Recalls & Warnings

8/15/2020

FTC Warns 20 More Companies for Coronavirus Claims

On August 14, 2020, the FTC announced that it sent warning letters to 20 companies for selling products such as vitamin C, hydrochloroquine, omega 3, and melatonin with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

10/06/2005

Deceptive Marketing of “Supreme Greens" -- Settlement with FTC

On October 6, 2005, the Federal Trade Commission (FTC) announced that three individuals and two companies have settled FTC charges over their roles in the deceptive marketing of Supreme Greens, an herbal supplement.

Recalls & Warnings

3/09/2022

FDA Warns Seller of Magnesium, CBD, Herbal Extracts & More

On February 9, 2022, the FDA issued a warning letter to Bea Lydecker’s Naturals, Inc.

Recalls & Warnings

9/11/2015

Thirteen Manufacturers Ordered to Stop Selling Devil's Claw Supplements

On September 9, 2015, the New York State Attorney General ordered 13 manufacturers, including Thorne Research Inc., NBTY, Inc. (Puritan's Pride) Inc., and Now Foods, to stop selling devil's claw supplements which were found to contain the incorrect species of the plant.

Recalls & Warnings

5/19/2020

FTC Sends Refund Checks to Consumers of Unproven Weight Loss and Sexual Enhancement Supplements

On May 19, 2020, the FTC announced it is mailing 143,636 checks totaling more than $8,500,000 to consumers who purchased deceptively marketed supplements.

News Release

2/25/2020

Top-rated Vitamin and Supplement Brands and Merchants for 2020 Based on Consumer Satisfaction -- Results of the ConsumerLab.com Survey of Vitamin & Supplement Users

White Plains, New York, February 25, 2020 — Each year, ConsumerLab.com surveys its free e-newsletter subscribers about the vitamins and supplements that they use. The results below are based on 9,782 responses collected in late November and early December 2019.

News Release

10/04/2019

ConsumerLab Tests Reveal Best Collagen Supplements for Wrinkles and Joints

White Plains, New York, October 4, 2019 — Collagen supplements are promoted to reduce wrinkles and decrease joint pain and stiffness, but do they really work, and if so, which products on the market provide the best quality collagen and the best value? To find out, ConsumerLab carefully ...

News Release

2/25/2019

Top-rated Vitamin and Supplement Brands and Merchants for 2019 Based on Consumer Satisfaction -- Results of the ConsumerLab.com Survey of Vitamin & Supplement Users

White Plains, New York, February 25, 2019 — Each year, ConsumerLab.com surveys its free e-newsletter subscribers about the vitamins and supplements that they use. The results below are based on 10,931 responses collected in late November and early December 2018.

News Release

1/03/2019

ConsumerLab Tests Reveal the Best Protein Powders, Shakes and Drinks -- 20% of Protein Powders and Drinks Fail CL's Tests of Quality

White Plains, New York, January 3, 2019 — Combined with resistance exercise, protein supplements can help athletes build muscle and older people prevent muscle loss. They can also help people with diabetes maintain blood sugar levels when consumed as part of a low-calorie diet.

News Release

2/25/2018

Top-rated Vitamin and Supplement Brands and Merchants for 2018 Based on Consumer Satisfaction

White Plains, New York, February 25, 2018 — Each year, ConsumerLab.com surveys its free e-newsletter subscribers about the vitamins and supplements that they use. The results below are based on 11,446 responses collected in late November and early December 2017.

News Release

2/25/2017

Top-rated Vitamin and Supplement Brands and Merchants for 2017 Based on Consumer Satisfaction

White Plains, New York, February 25, 2017 — Each year, ConsumerLab.com surveys its free e-newsletter subscribers about the vitamins and supplements that they use. The results below are based on 9,505 responses collected in late November and early December 2016.

News Release

12/06/2016

Which Brands of Alpha Lipoic Acid are Best? -- ConsumerLab.com Tests Lipoic Acid Supplements for Quality, Identifying Top Picks

White Plains, New York, December 6, 2016 — Alpha-lipoic acid supplements may improve insulin sensitivity and blood sugar control in people with type 2 diabetes, reduce symptoms of diabetic peripheral neuropathy, and enhance weight loss when dieting.

News Release

10/11/2016

What Are the Benefits of Resveratrol and Which Brands Are Best? -- ConsumerLab.com Reviews the Evidence and Tests the Quality of Popular Resveratrol Supplements

White Plains, New York, October 11, 2016 — Resveratrol supplements have been popular since 2006, when studies in animals showed "life-extending" and "endurance-enhancing" effects, among other potential benefits.

Recalls & Warnings

5/29/2021

FDA, FTC Warns Five Sellers of "Infertility" Supplements

The FDA and FTC (Federal Trade Commission) sent warning letters to the following five companies in May for illegally selling dietary supplements promoted with claims to treat infertility and other reproductive health issues:

Recalls & Warnings

3/14/2011

22 Brands of Whey Protein Recalled Due to Salmonella Concern

The FDA posted a recall notice involving 22 brands of whey protein powder due to potential contamination with salmonella. The recall was voluntarily initiated on March 10, 2011 by the manufacturer of the products, Vitalabs, Inc.

Recalls & Warnings

4/09/2003

Recall of Dangerous Sexual Enhancement Supplement Illegally Containing Viagra Ingredient

On April 4, 2003, the U.S. Food and Drug Administration's MedWatch program announced that Ultra Health Laboratories, Inc. and Bionate International, Inc. are warning consumers not to purchase or consume a product known as Vinarol tablets.

Recalls & Warnings

11/26/2019

FDA Warns Companies Selling CBD Products as Dietary Supplements

On November 25, 2019, the FDA issued warning letters to 15 companies for selling products containing CBD (cannabidiol) labeled and marketed as dietary supplements, and/or for making drug claims about these products.

Recalls & Warnings

12/27/2019

Federal Court Shuts Down Three Supplement Companies With Serious Manufacturing Violations

Update: (1/23/20) ABH has issued a recall of all its products, which are sold under various brand names by over 800 distributors and retailers. More details are available in CL's post about this recall.

Recalls & Warnings

4/16/2019

DMHA and Phenibut Are Not Permitted in Dietary Supplements, Warns FDA

On April 16, 2019, the FDA announced it has issued 11 warning letters to companies whose dietary supplement products contain the drugs DMHA or phenibut, and therefore are in violation of the law.

News Release

2/25/2016

Top-rated Vitamin and Supplement Brands and Merchants for 2016 Based on Consumer Satisfaction

Each year, ConsumerLab.com surveys its free e-newsletter subscribers about the vitamins and supplements that they use. The results below are based on 11,534 responses collected in November, 2015. Respondents gave ratings for 963 brands and 399 merchants.

News Release

2/25/2015

Top-rated Vitamin and Supplement Brands and Merchants for 2015 Based on Consumer Satisfaction -- Results of the ConsumerLab.com Survey of Vitamin & Supplement Users

Each year, ConsumerLab.com surveys its free e-newsletter subscribers about the vitamins and supplements that they use. The results below are based on 10,329 responses collected in November, 2014. Respondents gave ratings for 1,709 brands and 891 merchants.

News Release

5/07/2014

Flaxseed and Other Popular Seed Oil Supplements Tested by ConsumerLab.com, But Not All Brands Pass -- Flaxseed, Black Currant, Borage and Evening Primrose Oils Reviewed

White Plains, New York, May 7, 2014 — Plant seed oils are popular supplements that provide omega-3 and omega-6 fatty acids, but which products offer the best value and quality? Recent analyses by ConsumerLab.

News Release

2/12/2014

Top-rated Vitamin and Supplement Brands and Merchants for 2014 Based on Consumer Satisfaction -- Results of the ConsumerLab.com Survey of Vitamin & Supplement Users

Each year, ConsumerLab.com surveys its free e-newsletter subscribers about the vitamins and supplements that they use. The results below are based on 10,326 responses collected in November, 2013. Respondents gave ratings for 1,639 brands and 788 merchants.

News Release

6/11/2013

31% of Protein Powders and Drinks Fail Tests by ConsumerLab.com

White Plains, New York — June 11, 2013 — What's really in a scoop of "protein powder"? sIn some products, a lot less protein or a lot more carbohydrates than you would expect, and perhaps even a serving of something you don't want -- lead. That's according to recent tests by ConsumerLab.

Recalls & Warnings

8/01/2022

53 Protein, Meal Replacement and Nutritional Beverages Recalled Due to Bacterial Contamination

On July 29, 2022, Lyons Magnus LLC issued a recall of 53 protein, meal replacement, and nutritional beverages, including those sold under the brand names of Glucerna, Premier Protein, Oatly, and others, due to the potential for microbial contamination, including from Cronobacter sakazakii.

Recalls & Warnings

2/01/2018

Seller of Supplements for Opiate Withdrawal Warned for Drug Claims

On January 11, 2018, the FDA sent warning letters to ten sellers of supplements promoted to treat opiate withdrawal following reviews of the companies' websites and social media which found statements and testimonials made about the products to be drug claims.

Recalls & Warnings

5/09/2020

FTC Warns 45 More Companies for Coronavirus Claims

On May 7, 2020, the FTC announced that it sent warning letters to 45 companies for selling products such as herbal products, immune system boosters, and vitamin C with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

5/23/2020

FTC Warns 50 More Companies for Coronavirus Claims

On May 21, 2020, the FTC announced that it sent warning letters to 50 companies for selling products such as herbal products, immune system boosters, and vitamin C, with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

8/25/2022

Oregon’s Wild Harvest Warned by FDA for Manufacturing Violations

On July 8, 2022, the FDA issued a warning letter to Oregon’s Wild Harvest, Inc.

Recalls & Warnings

11/21/2022

Healthy Sense and People’s Choice Multis Recalled

On November 17, 2022, Mason Vitamins Inc.

Recalls & Warnings

12/01/2022

FTC Takes Action Against Company Promoting “COVID Resist” Supplement to Treat COVID-19

On November 22, 2022, the FTC filed a complaint in a U.S. district court against California-based company Precision Patient Outcomes, Inc. for promoting its COVID Resist and VIRUS Resist supplements to prevent and treat COVID-19.

Recalls & Warnings

6/08/2022

Allergy Bee Nasal Swabs Recalled Due to Potential Contamination With Yeast, Mold & Bacteria

On June 7, 2022, Buzzagogo, Inc. issued a nationwide recall of one lot of Allergy Bee Gone for Kids Nasal Swab Remedy after FDA testing revealed elevated levels of yeast and mold. The agency also warned the recalled swabs may contain the bacteria Bacillus cereus.

Recalls & Warnings

6/02/2022

Prune & Senna Softgels Recalled Due to Undeclared Peanuts

On March 26, 2022, Indiana Botanic Gardens Inc. issued a voluntary recall of one lot of Botanic Choice brand Prune & Senna Softgels because the product contained undeclared peanuts.

Recalls & Warnings

2/10/2022

Three Sexual Enhancement Supplements Sold on Amazon Recalled

On February 8, 2022, specific lots of three male sexual enhancement supplements, Red Mammoth capsules, MAC DADDY RED capsules, MAC DADDY PURPLE capsules, and The Red Pill capsules, were recalled because Amazon laboratory analyses found them to contain undeclared ...

News Release

2/01/2013

Top-rated Vitamin and Supplement Brands and Merchants for 2013 Based on Consumer Satisfaction

Each year, ConsumerLab.com surveys its free e-newsletter subscribers about the vitamins and supplements that they use. The results below are based on 10,862 responses collected in November, 2012. Respondents gave ratings for 1,438 brands and 851 merchants.

Recalls & Warnings

10/15/2012

Recall of Nutrition Bars Containing Peanut Butter Due To Salmonella Risk

On October 11 and 12, 2012, four brands of nutrition bars were voluntarily recalled due to possible salmonella contamination of the peanut butter used in each of these bars. The peanut butter was produced by Sunland Inc., and is part of a larger recall of Sunland's peanut butter and peanut products.

Recalls & Warnings

5/14/2021

Maker of Care by Design CBD Settles Charges of Unsupported Claims

On May 5, 2021, Cannacraft, Inc.

Recalls & Warnings

5/10/2021

Collagen & Biotin Supplement Recalled Due to Allergen Risk

On May 6, 2021, Bloommy, Inc. issued a recall of Bloommy Biotin Collagen Keratin Capsules for Skin, Joint, and Hair due to the presence of a fish allergen for the collagen-based ingredient.

Recalls & Warnings

5/08/2021

FDA Warns Seller of Vitamins B12, C, D, and K

On April 7, 2021, the FDA issued a warning letter to Unived Inc following a review of the company's websites, which found statements made about the company's products Unived brand Colox, CalDveg, B12+D3, and D3+K2-7 to be drug claims.

Recalls & Warnings

7/10/2021

FDA Warns Seller of Omega XL

On June 31, 2021 the FDA issued a warning letter to Great Healthworks, Inc. following a review of the company's website, which found statements made about Omega XL and ProbioticXL supplements to be drug claims.

Recalls & Warnings

6/22/2021

Living Free Vitamins, Joint, Nerve and Other Supplements Recalled

On June 21, 2021, Bea Lydecker's Naturals, Inc. issued a recall of six Living Free brand supplements because the labels do not declare soy lecithin.

Recalls & Warnings

6/22/2021

Prairie Wolf Hand Sanitizer Recalled

On June 21, 2021, Prairie Wolf Spirits, Inc. recalled all lots of Prairie Wolf Distillery hand sanitizer packaged in 16.9 fluid ounce and 20 fluid ounce containers that resemble water bottles because the products pose a risk of ingestion.

Recalls & Warnings

1/19/2022

FDA Warns Seller of Carnitine and Alpha Lipoic Acid Supplements

On November 18, 2021, the FDA issued a warning letter to GeroNova Research Inc.

Recalls & Warnings

1/12/2022

FDA Warns Consumers Not to Use LuSys Laboratories COVID Tests Due to False Results

Update: (03/09/22) On February 17, 2022, the FDA issued a warning letter to LuSys Laboratories, Inc.

Recalls & Warnings

1/03/2022

Seller of Wormwood, Aloe Supplement Warned by FDA

On December 7, 2021, the FDA issued a warning letter for Western Herb Products, Inc.

Recalls & Warnings

12/01/2021

Probiotics Recalled Due to Bacterial Contamination, May Be Life-Threatening to Some

On December 1, 2021, Livia Global, Inc issued a voluntary recall of two lots of probiotics due to potential contamination with Pseudomonas aeruginosa. This bacterium, if ingested, can cause life-threatening infection in immunocompromised individuals.

Recalls & Warnings

11/24/2021

FDA Warns Sanitizer Corporation For Manufacturing and Misbranding Violations

On September 24, 2021, the FDA issued a warning letter to Chameleon Beverage Co. Inc.

Recalls & Warnings

3/30/2021

Real Water Alkaline Water Recalled for Possible Link to Liver Illness

On March 24, 2021, Real Water, Inc. recalled all sizes of Real Water bottled alkaline water because it may be linked to multiple cases of non-viral hepatitis that occurred in Las Vegas, NV in November of 2020.

Recalls & Warnings

2/22/2021

FDA Warns Sellers of St. John's Wort

On February 18, 2021, the FDA issued warning letters to two companies following reviews of the companies' websites, which found statements made about the companies' St. John's Wort products to be drug claims. These products include St.

Recalls & Warnings

2/16/2021

Seller of BioCBD+ Products Warned for COVID-19 and Drug Claims

On February 11, 2021, the FDA issued a warning letter to Evolved Ayurvedic Discoveries, Inc.

Recalls & Warnings

3/16/2021

FDA Warns Seller of Essential Oils

On March 12, 2021, the FDA issued a warning letter to Ravenscroft Apothecary, Inc.

Recalls & Warnings

3/05/2021

FTC Takes Further Action Against Deceptive CBD Claims

On March 5, 2021, the Federal Trade Commission (FTC) announced that it has approved final administrative consent orders against six companies for selling CBD products with unsupported and deceptive health claims that they can treat a variety of conditions, including cancer, heart disease, ...

Recalls & Warnings

4/23/2019

"Brain Boosting" Supplements Were Promoted With Non-Existent Clinical Studies

On April 10th, 2019, the FTC (Federal Trade Commission) announced the marketers of cognitive enhancement supplements Geniux, Xcel, EVO, and Ion-Z have agreed to settle charges that they made false claims about the product, including fake research references and celebrity ...

Recalls & Warnings

5/01/2021

Hand Sanitizer Sold at Ulta, TJ Maxx, and Marshalls Recalled Due to Toxic Chemicals

On April 28, 2021, Scentsational Soaps & Candles, Inc.

Recalls & Warnings

4/06/2022

Mandalorian and Mickey Mouse Hand Sanitizers Recalled Due to Benzene, Methanol

On April 1, 2022, Best Brands Consumer Products, Inc.

Recalls & Warnings

5/09/2022

FDA Warns Five Companies for Selling CBD Supplements, Gummies and Creams With Delta-8 THC

On May 4th, 2022, the FDA issued warning letters to five companies for selling CBD and other products labeled as containing delta-8 tetrahydrocannabinol (delta-8 THC).

Recalls & Warnings

5/11/2022

FDA Warns 10 Companies for Selling Workout Supplements With Dangerous Ingredients

On May 4, 2022, the FDA issued warning letters to 10 companies for selling products promoted for muscle building, fat burning and other uses that contain potentially dangerous ingredients not permitted in dietary supplements, including hordenine, higenamine, 5-alpha-hydroxy-laxogenin, and CBD.

Recalls & Warnings

7/22/2022

FDA Warns Seller of Vision, Calcium & Magnesium Supplements and More

On June 14, 2022, the FDA issued a warning letter to New Sun Inc. following inspection of the company’s website which found statements about the company’s products to be drug claims.

News Release

2/01/2012

Top-rated vitamin and supplement brands and merchants on consumer satisfaction for 2012 -- Based on ConsumerLab.com Survey of Vitamin & Supplement Users

Each year, ConsumerLab.com surveys its free e-newsletter subscribers about the vitamins and supplements that they use. The results below are based on 10,260 responses collected in November, 2011. Most respondents used multiple supplements.

Recalls & Warnings

2/02/2021

FDA Warns Seller of Reishi Mushroom Supplements

On January 6, 2021, the FDA issued a warning letter to Entia Biosciences, Inc following a review of the company's website, which found statements made about the company's products Lion's Mane - All Natural Supplement, Antrodia Mushroom Powder, Maitake Mushroom Powder, Reishi ...

Recalls & Warnings

1/31/2021

Protein and Fiber Bars Recalled Due to Allergen Risk

On January 28, 2021, think! and Interpac Technologies, Inc. issued a voluntary recall of think! Protein + Fiber Oatmeal: Farmer's Market Berry Crumble due to the potential presence of tree nuts, including almonds and pecans.

Recalls & Warnings

1/20/2021

FDA Warns Seller of Vitamin D, Curcumin and CoQ10 Promoted for Treating COVID-19

On December 28, 2020, the FDA issued a warning letter to Smarter Nutrition, Inc. following a review of the company's website, which found statements made about the company's products Smarter Curcumin, Smarter Ubiquinol, and Smarter Vitamin D3 to be drug claims.

Recalls & Warnings

1/12/2021

FDA Warns Seller of Joint and Hair Loss Products

On December 22, 2020, the FDA issued a warning letter to Speedwinds Nutrition, Inc. following a review of the company's website, which found statements made about the company's products Synotrex and Sephren to be drug claims.

Recalls & Warnings

6/16/2020

FDA Warns Four Companies for Unsafe "Homeopathic" Injectables

On June 16, 2020, the FDA issued warning letters to four manufacturers of unapproved injectable drugs labeled as homeopathic.

Recalls & Warnings

6/09/2020

Six More Multi-Level Marketing Companies Warned for Coronavirus and Deceptive Earnings Claims

On June 5, 2020, the FTC announced that it sent warning letters to six multi-level marketing companies for selling products such as immune system boosters and probiotics with unsupported claims that they can treat coronavirus (COVID-19) and/or for misrepresenting potential earnings people who have ...

Recalls & Warnings

6/30/2020

FDA Warns Seller of Alpha Lipoic Acid, Berberine, and More

On June 18, 2020, the FDA issued a warning letter to Only Natural, Inc. dba Bio Nutrition, Inc.

Recalls & Warnings

8/13/2020

FDA Warns Three More Companies Selling Unapproved COVID-19 Tests

Between July 23 and 24, the FDA issued warning letters to three companies for marketing unapproved, adulterated or misbranded antibody tests for coronavirus (COVID-19).

Recalls & Warnings

11/10/2020

FDA Warns Seller of Digestive Enzymes, Nattokinase, and More

On October 27, 2020, the FDA issued a warning letter to World Nutrition, Inc.

Recalls & Warnings

11/02/2020

Silver Cannot Be Promoted to Prevent or Treat COVID-19

On October 30, 2020, the FDA issued a warning letter to Spartan Enterprises Inc. dba Watershed Wellness Center for selling the silver product Dissolve BioActive Silicate with unsupported claims that it can treat coronavirus (COVID-19).

Recalls & Warnings

10/15/2020

FDA Warns Five Sellers of Dangerous Cesium Salt Supplements

On October 9, the FDA issued warning letters to five companies for selling products containing cesium chloride. The FDA has previously warned consumers not to use dietary supplements containing cesium chloride or any other cesium salt.

Recalls & Warnings

9/11/2020

Seller of "COVID PACK" Warned for Coronavirus Claims

On September 9, 2020, the FDA issued a warning letter to Pharmacy Plus, Inc. dba Vital Care Compounder for selling COVID PACK and COVID 'POSITIVE' PACK products with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

9/08/2020

Seller of "Diabetes Supplement" & More Warned for Drug Claims

On August 25, 2020, the FDA issued a warning letter to Nutritional Supplements Corporation Inc following a review of the company's website, which found statements made about some of the company's products, including Vitadone, Diabrex, and Viadevita to be drug claims.

Recalls & Warnings

9/08/2020

FDA Warns Seller of Multivitamin for Manufacturing Violations

On August 14, 2020, the FDA issued a warning letter to Revival Products, Inc.

Recalls & Warnings

2/29/2008

FTC Sues Sellers of Weight-Loss Pills for False Advertising

On February 8, 2008 the The Federal Trade Commission (FTC) charged a business operation with violating federal law by falsely claiming that its weight-loss pills cause users to lose weight without dieting or exercise.

Recalls & Warnings

6/04/2004

FTC Charges Marketers of Two Supplements with False Claims to Cure Range of Diseases

On June 3, 2004 the Federal Trade Commission (FTC) charged marketers of two dietary supplements with falsely claiming that their products can prevent and cure cancer and other diseases. According to the FTC’s complaint, Boston-area marketers Direct Marketing Concepts, Inc. (DMC), ITV Direct, Inc.

Recalls & Warnings

1/18/2002

Recall of Pepsin-containing Digestive Supplements

The U.S. Food and Drug Administration (FDA) released the following Class I recall information in its January 16, 2002 Enforcement Report.

Recalls & Warnings

1/23/2020

Massive Recall of Supplements Sold by Over 800 Brands

On January 21, 2020, a group of contract manufacturers of dietary supplements issued a recall affecting products sold by over 800 brands that sell the products under their own brand names and labels.

Recalls & Warnings

2/19/2019

Alaskan Smoked Silver Salmon in Jars and Cans Recalled Due to Risk of Botulism

On February 15, 2019, Smoked Alaska Seafoods, Inc. recalled all jars and cans of Smoked Silver Salmon because it has the potential to be contaminated with Clostridium botulinum, a bacterium which can cause life-threatening illness or death.

Recalls & Warnings

12/24/2020

Wash-Free Hand Sanitizer With Potentially Toxic Ingredient Recalled

On December 23, 2020, Shane Erickson, Inc.

Recalls & Warnings

12/17/2020

FTC Crackdown on Six Deceptive CBD Products

On December 17, 2020, the FTC announced that it is taking action against six companies for selling CBD products with unsupported and deceptive health claims that they can treat a variety of conditions, including cancer, heart disease, hypertension, Alzheimer's disease, and others.

Recalls & Warnings

10/06/2020

FDA Warns Seller of Red Yeast Rice, Vitamin D, Blood Pressure Supplements, and More

On August 28, 2020, the FDA issued a warning letter to Dr. Sam Robbins, Inc.

Recalls & Warnings

10/12/2005

Supplement Company to Pay $2 Million Penalty For Alleged Violations of FTC Order

On October 12, 2005 the Federal Trade Commission (FTC) announced that under the terms of a consent decree approved by the it for submission by the U.S. Department of Justice (DOJ) to the federal court for approval, NBTY, Inc. (NBTY, formerly Nature’s Bounty, Inc.

Recalls & Warnings

4/19/2007

Recall of Another Sex Enhancement Supplement

On April 17, 2007 the Food and Drug Administration (FDA) website posted an announcement that Jen-On Herbal Science International, Inc. is conducting a voluntary nationwide recall of the company's supplement product sold under the name H S Joy of Love. Jen-On Herbal Science International, Inc.

Recalls & Warnings

12/17/2004

FDA Seizes Ginseng Because of Potentially Risky Pesticide Residues

On December 16, 2004, the Food and Drug Administration (FDA) announced that the U.S. District Court for the District of New Jersey issued a warrant for the seizure of imported ginseng held for sale at FCC Products, Inc., located in Livingston, N.J. The U.S.

Recalls & Warnings

7/01/2003

Direct Marketers of Weight Loss, Impotence, and Arthritis Supplements Charged with Deceptive Claims

On July 1, 2003, the Federal Trade Commission (FTC) announced three enforcement actions against direct marketers of weight-loss products containing ephedra. The two settlements and one complaint, filed in U.S.

Recalls & Warnings

11/15/2009

Nationwide Recall of a Weight Loss Supplement Found to Contain Undeclared Drug Ingredients

On November 12, 2009, The U.S. Food and Drug Administration (FDA) announced that it informed GMP Herbal Products, Inc. that its product "Pai You Guo," a weight loss dietary supplement, contains undeclared drug ingredients.

Recalls & Warnings

8/11/2015

Company Ordered to Stop Making and Selling Supplements

On August 4, 2015, a federal court ordered a permanent injunction against dietary supplement company Atrium Inc., and two companies under the same ownerhship, Aspen Group Inc., Nutri-Pak of Wisconsin Inc.

Recalls & Warnings

3/31/2018

Supplement Manufacturer Shut Down for Manufacturing Violations

On March 29, 2018, the FDA announced that U.S. District Court for the Eastern District of New York has entered a consent decree of permanent injunction with Riddhi USA, Inc. and Mohd M. Alam, president and owner of Riddhi USA, Inc., for selling adulterated and misbranded dietary supplements.

Recalls & Warnings

1/10/2013

FDA Warns Aloe and Herbal Supplement Companies For Manufacturing Violations

AloeScience Labs, Inc. -- On November 14, 2012, the FDA issued a warning letter to AloeScience Labs, Inc.

Recalls & Warnings

4/21/2011

FTC Targets Fake News Sites Making Deceptive Acai Claims

On April 19, 2011, the Federal Trade Commission (FTC) requested federal courts to temporarily halt the allegedly deceptive tactics of 10 operations using fake news websites to market acai berry weight-loss products.

Recalls & Warnings

8/02/2012

FDA Warns Two Supplement Makers of Manufacturing Violations

On July 19, 2012, the FDA issued a warning letter to H & L Jerch Sales, Inc. for failing to maintain written quality control procedures, which constitutes a violation of current Good Manufacturing Practices (cGMP) and caused the company’s products to be declared adulterated.

Recalls & Warnings

7/05/2012

FDA Warns Good Herbs Inc. of Manufacturing Violations and Drug Claims

The FDA issued a warning letter to Good Herbs Inc. on May 24, 2012, after a facility inspection found the company to be in violation of current manufacturing regulations, including lack of documentation and written procedures.

Recalls & Warnings

3/19/2004

Seasilver Stopped from Making Claim to Cure "Over 650" Diseases

On March 17, the Food and Drug Administration (FDA) announced that Seasilver USA, Inc., and Americaloe, Inc.

Recalls & Warnings

4/11/2008

Twelve Dietary Herbal Supplements Recalled -- Possible Health Risk Associated with Ephedra, Aristolochic Acid and Human Placenta

On April 10, 2008, the FDA posted a recall notice issued the same day from Herbal Science International, Inc. (AKA Jen-On Herbal Science International, Inc.).

Recalls & Warnings

10/18/2005

FTC Stops False Claims about HGH Oral Spray

On October 18, 2005, the Federal Trade Commission (FTC) announced that, at its request, a federal court issued a temporary restraining order against marketers of oral sprays that supposedly contain human growth hormone (HGH) to stop them from making alleged false and deceptive claims and from ...

Recalls & Warnings

4/01/2004

Aloe Producer Recalls Product Due to Toxic Levels of Vitamin D

On March 26.2004, the Food and Drug Administration (FDA) announced that Aloe Commodities International, Inc., Carrollton, Texas, is recalling 1600 bottles of Solutions IE Ageless Formula II, Lot numbers P2207 and P2221 because they contain a significantly higher-than-labeled level of vitamin D3.

Recalls & Warnings

10/06/2011

Testosterone Booster Supplement Recalled for Containing Synthetic Steroid

On October 5, 2011, the U.S. FDA announced that Superior Metabolic Technologies Inc of Marietta, Georgia is voluntarily recalling all lots of the testosterone booster Uprizing 2.

Recalls & Warnings

8/31/2009

Court Orders Marketers of Supreme Greens and Coral Calcium to Pay Nearly $70 Million for Consumer Refunds

On August 27, 2009, a federal district court ordered the marketers of two dietary supplements – "Supreme Greens" and "Coral Calcium" – who claimed the products would cure ailments ranging from cancer and Parkinson’s disease to heart disease and autoimmune diseases to pay nearly $70 million for ...

Recalls & Warnings

10/30/2014

Seller of Vitamin C, Iron and Detox Supplements Warned for Violations, Drug Claims

On October 16, 2014, the FDA issued a warning letter to Vitalab Co., Inc. (which manufactures and labels supplements for three distributors: V.E. Irons, Inc., Springreen Products, Inc., and Sonne's Organic Foods, Inc.

Recalls & Warnings

12/01/2017

Nutra Labs Recalls Sexual Enhancement Supplements Containing Undeclared Drugs

On November 30, 2017, Nutra Labs Inc. recalled certain lots of its sexual enhancement supplements Bull 1800 mg Capsules and Chao Jimengnan 150 mg Tablets because they were found to contain undeclared sildenafil.

Recalls & Warnings

7/31/2020

FDA Warns Seven Sellers of "Hangover Cures"

The FDA recently issued warning letters to seven companies for promoting hangover relief products with drug claims (use the links below to read the full warning letter):

Recalls & Warnings

8/14/2020

The Green Herb and New Genesis Health Warned for Manufacturing Violations

On July 31, 2019, the FDA issued a warning letter to Davis Ventures, Inc.

Recalls & Warnings

6/23/2020

BioPure Healing Products Warned for Manufacturing Violations

On June 17, 2020, the FDA issued a warning letter to BHP Holdings Inc.

Recalls & Warnings

3/05/2020

Protein Powder Recalled Due to Undeclared Milk

On March 3, 2020, New Capstone, Inc. issued a recall of ReStructure Vanilla Protein Powder because it may contain undeclared milk.

Recalls & Warnings

7/28/2022

FDA Warns Three Manufacturers of Sanitizer for Manufacturing and Misbranding Violations

Between July 8 and July 21, the FDA issued warning letters to three companies selling hand sanitizer products that violate Current Good Manufacturing Practices (cGMP), are adulterated and misbranded, and for refusal to allow the agency to access and copy company records.

Recalls & Warnings

11/21/2022

6 Supplement Companies Warned by FDA for Making Cholesterol Claims

On May 4, 2022, the FDA issued warning letters to six supplement companies following review that found statements made on company websites and Walmart purchase pages suggesting the products could lower cholesterol to be drug claims, which are not permitted for dietary supplements.

Recalls & Warnings

11/28/2022

Seller of Joint Health, Collagen Protein and More Warned for Drug Claims

On November 14, 2022, the FDA issued a warning letter to The Truth Company, LLC (parent company of Kinobody, LLC and UMZU, LLC) following inspection of the company’s websites which found statements about its Betaine, Immune, Redwood, Sensolin, Thyrite, zuRelief, Kino Aminos, Kino Collagen ...

Recalls & Warnings

1/12/2023

FDA Warns Two Sellers Promoting CBD to Treat COVID-19

On January 10, 2023, the FDA issued warning letters to two companies following a review that found statements made on the companies’ websites to be drug claims because they promoted the cannabidiol (CBD) products to prevent or treat COVID-19.

Recalls & Warnings

4/05/2022

Sexual Enhancement Capsules for Men Recalled

On April 1, 2022, F&S Medical Supply, dba Pink Toyz, recalled one lot of Pink Pussycat 3000 mg capsules to the consumer level because FDA analysis found them to contain sildenafil.

Recalls & Warnings

3/09/2022

Court Bars Salud Natural From Selling Aloe, Joint Supplements & More

On March 8, 2022, a federal court ordered Salud Natural Entrepreneur, Inc. to stop distributing nutritional supplements that violate the Federal Food, Drug and Cosmetic Act (FDCA).

Recalls & Warnings

7/21/2022

UV Light Wands That May Cause Injury, According to the FDA

The FDA recently warned consumers of potential exposure to unsafe levels of ultraviolet-C (UV-C) radiation associated with the use of certain brands of ultraviolet (UV) wands, as found from testing conducted by the agency.

Recalls & Warnings

7/01/2022

Male Enhancement Supplements Sold on Amazon Recalled

On January 27, 2022, Loud Muscle Science LLC issued a voluntary recall of various lots of Launch Sequence supplements because they were found to contain the prescription drug Tadalfil.

Recalls & Warnings

6/16/2022

Omega 3 Supplements Recalled Due to Undeclared Drug Ingredients

On May 28, 2022, Latin Foods Market issued a voluntary recall of one lot of Artri King Reforzado con Ortiga y Omega 3 tablets after FDA laboratory analysis found the presence of undeclared diclofenac and dexamethasone.

Recalls & Warnings

5/20/2014

FTC Charges Seller of Green Coffee Bean with False Weight Loss Claims, Fake Websites

On May 15, 2014, the Federal Trade Commission (FTC) filed a lawsuit against the sellers of Pure Green Coffee for making unsubstantiated weight loss claims and deceiving consumers with fake "news" websites.

Recalls & Warnings

4/17/2015

Herbal Laxative and "Detox" Kit Containing High Levels of Lead and/or Arsenic Recalled in Canada

On April 15, 2015, Health Canada (the Canadian equivalent of the U.S. FDA) announced that St. Francis Herb Farm Inc.

Recalls & Warnings

10/17/2013

Turmeric Spice Powder Recalled Due To High Lead Levels

On October 3, 2013, the OnTime Distribution Inc. issued a voluntary recall of PRAN brand spice powder Turmeric because it was found to contain high levels of lead.

Recalls & Warnings

1/09/2014

Marketers of "Genetically Customized" Supplements Settle FTC Charges of Deceptive Health Claims

Two marketers of "genetically customized" nutritional supplements have agreed to a settlement with the Federal Trade Commission (FTC) over charges that the companies made deceptive advertising claims and did not adequately protect customers' medical and financial information.

Recalls & Warnings

11/05/2021

Herb Recalled Due to Risk of Lead, Cadmium Contamination

On November 2, 2021, Murray Int'l Trading issued a recall of Herbal Doctor brand Angelicae Sinensis due to potential risk it may contain elevated levels of lead and cadmium.

Recalls & Warnings

5/04/2021

CytoSport's Evolve Protein Shakes Recalled

On May 1, 2021, CytoSport, Inc., recalled certain lots of Evolve Protein Shakes because they have the potential to be contaminated with soy protein.

Recalls & Warnings

3/04/2021

Federal Court Bars Confidence USA from Selling Supplements

On March 4, 2021, the FDA announced a permanent injunction has been entered, barring dietary supplement manufacturer Confidence USA Inc. and two of its executives from producing or selling products until they become compliant with current good manufacturing practices (cGMPs).

Recalls & Warnings

1/31/2017

Vegetarian Protein Drink Recalled Due to Undeclared Milk

On January 28, 2017 NSE Products, Inc. (a subsidiary of Nu Skin Enterprises, Inc.) issued a recall of its vegetarian ageLOC TR90 Protein Boost protein drink because it contains undeclared milk.  

News Release

3/13/2006

ConsumerLab.com reports on supplements for bone health containing calcium and vitamin D— Results posted for 32 supplements for adults and children; One found contaminated with lead

WESTCHESTER COUNTY, NEW YORK — MARCH 13, 2006 — ConsumerLab.com announced test results today from its new Product Review of Supplements for Bone Health covering 32 adult and children's products containing calcium and vitamin D. Sales of calcium supplements in the U.S.

News Release

4/27/2005

ConsumerLab.com finds quality of most nutrition powders and drinks high, but identifies five protein powders with excess sodium or cholesterol — Report Now Available Online

WHITE PLAINS, NY — APRIL 27, 2005 — ConsumerLab.com has released its latest report on the quality of nutrition powders, shakes and drinks. These products are used for general nutrition, dieting, and meal-replacement and are frequently used by athletes and bodybuilders.

News Release

5/28/2004

ConsumerLab.com warns of deceptive campaign by manufacturer of children's vitamin

WHITE PLAINS, NY — FOR IMMEDIATE RELEASE — FRIDAY MAY 28, 2004 — Responding to a deceptive public relations campaign recently launched by vitamin manufacturer Northwest Natural Products, Inc., ConsumerLab.

News Release

12/30/2002

Top quality melatonin products identified by ConsumerLab.com — Hormone supplement used to treat sleep disturbances due to jet travel and other causes

WHITE PLAINS, NY — December 30, 2002 — In its latest Product Review, ConsumerLab.com found that 16 of 18 melatonin dietary supplements met their label claims and were free of lead contamination.

News Release

10/29/2002

Enormous variation found in strength of garlic supplements — most popular herb in U.S. — ConsumerLab.com releases results online today

WHITE PLAINS, NY — October 29, 2002 — ConsumerLab.com's Product Review of Garlic Supplements found strength to vary by as much as 1500% across products. Strength was based on each product's ability to generate allicin, a chemical associated with the efficacy of non-aged garlic.

News Release

3/05/2002

ConsumerLab.com finds nutrition powders & drinks more accurately labeled than nutrition bars, but unapproved food ingredient seen in some

White Plains, NY -- March 5, 2002 — ConsumerLab.com announced today that 24 of 26 nutrition powders and drinks that it recently evaluated met their label claims for carbohydrates, fats, and proteins. This is in stark contrast to ConsumerLab.

Recalls & Warnings

11/23/2022

CBD Not Permitted in Gummies, Candies, Cookies, Candy, or Pet Treats, Says FDA

On November 16, 2022, the FDA issued warning letters to five companies for selling products such as gummies, tea, cookies, lollipops, fruit snacks, hard candies, and pet treats containing cannabidiol (CBD) and/or delta-8 tetrahydrocannabinol (delta-8 THC) as conventional food products.

Recalls & Warnings

12/27/2012

Two Supplement Companies Warned For Manufacturing Violations

Sterling USA Neutraceutical Lab, LLC -- On November 16, 2012, the FDA issued a warning letter to Sterling USA Neutraceutical Lab, LLC following a facility inspection which found the company’s dietary supplements to be adulterated because they were have been prepared, packed, or held under ...

Recalls & Warnings

11/08/2012

Chinese Herb Recalled Due To Undeclared Sulfites

On November 7, 2012, the New York State Department of Agriculture announced that Mayflower International Inc., aka Fu Xiang Yuan Trading Inc., is recalling Lily Dry after sample analysis revealed the product contains high levels of sulfites which were not declared on the label.

Recalls & Warnings

12/05/2015

FDA Warns Companies Selling Products Containing Picamilon

On November 30, 2015, the FDA issued warning letters to five supplement companies selling products containing picamilon, which is not a lawful dietary supplement ingredient in the U.S.

Recalls & Warnings

4/26/2015

FDA Identifies More Products Listing Synthetic Amphetamine

On April 22, 2015, the FDA issued warning letters to sellers of weight loss and workout supplements that list a synthetic, amphetamine-like compound called beta- methylphenylethylamine (BMPEA) on product labels.

Recalls & Warnings

7/13/2012

Alistrol Health Inc. Warned Over Health Claims on Products

On June 26, 2012, the FDA issued a warning letter to Alistrol Health Inc. for making product statements on the company's websites that constitute drug claims.

Recalls & Warnings

9/13/2010

Supplement for "Increasing Desire" Recalled for Containing Drug

The U.S. FDA posted a notice regarding the recall of Masxtreme Capsules by the distributor, Natural Wellness, Inc. FDA analysis has determined the product contains undeclared amounts of Aminotadalafil, an analog of tadalafil.

Recalls & Warnings

7/20/2010

Recall of ED Supplement Containing Drug

On July 20, 2010, the U.S. FDA posted a news announcement from Good Health, Inc. regarding the recall of Vialipro, a sexual enhancement supplement sold nationally.

Recalls & Warnings

10/05/2011

FDA Warns Nutrition Center Inc (Nutri-West) of Manufacturing Violations

The FDA published a Warning Letter dated September 9, 2011 to Nutrition Center Inc. (dba Nutri-West) informing the firm of manufacturing violations found during an inspection of the firm's facility in Douglas, Wyoming in April, 2011.

Recalls & Warnings

9/08/2011

FDA Warns Several Supplement Manufacturers Not Following Good Manufacturing Practices

In recent weeks, the U.S. FDA has sent warning letters to several supplement manufacturers regarding deficiencies identified during audits of their facilities and not adequately corrected. Use the links below to access the Warning Letters on the FDA website.

Recalls & Warnings

6/01/2012

Homeopathic Manufacturer Settles False Advertising Suit

June 1, 2012 — A federal court in California recently authorized the settlement of a class action lawsuit against Boiron Inc. and Boiron USA, Inc.

Recalls & Warnings

8/24/2012

Protein Shots, Drinks and Gelatin Recalled For Potential Botulism Contamination

On August 17, 2012, Protica Inc.

Recalls & Warnings

6/20/2003

FTC Charges Marketers of Seasilver with False and Deceptive Claims

On June 19, 2003, The Federal Trade Commission (FTC) and the Food and Drug Administration (FDA) announced coordinated actions against two companies - both charged with promoting the dietary supplement "Seasilver" with unsubstantiated medical claims. The agencies' actions against Seasilver USA, Inc.

Recalls & Warnings

1/24/2003

FTC Challenges Weight-loss Claims for Slim Down Solution

The Federal Trade Commission today charged Slim Down Solution, LLC, Maderia Management, Inc., and several related companies and individuals with using false and unsubstantiated claims in the marketing and advertising of "Slim Down Solution" - a purported weight-loss product.

Recalls & Warnings

10/05/2007

FTC Charges Progesterone Cream Sellers with Making Unsubstantiated Claims

On October 5, 2007 the Federal Trade Commission (FTC) announced complaints against seven online sellers of alternative hormone replacement therapy (HRT) products, alleging that they made health claims for their natural progesterone creams without supporting scientific evidence.

Recalls & Warnings

9/25/2007

Recall of Contaminated Baby Supplement

On September 21, 2007 the U.S. Food and Drug Administration (FDA) warned consumers not to consume Baby's Bliss Gripe Water, apple flavor, with a code of 26952V and expiration date of October 2008 (shown as '10/08' on the label). The product is distributed by MOM Enterprises, Inc.

Recalls & Warnings

8/09/2007

FDA Warning on Red Yeast Rice Products

On August 9, 2007, the U.S. Food and Drug Administration (FDA) warned consumers not to buy or eat three red yeast rice products promoted and sold on Web sites. The products may contain an unauthorized drug that could be harmful to health.

Recalls & Warnings

6/14/2007

Marketers of Bogus Growth Hormone Sprays Settle with FTC

On May 29, 2007 the Federal Trade Commission (FTC)announced that two operations that marketed oral sprays that were supposed to help users lose weight, reverse the aging process, and prevent or treat diseases have settled FTC charges that their claims were bogus.

Recalls & Warnings

1/19/2002

Recall of Certain Iron Supplements

The U.S. Food and Drug Administration (FDA) released the following Class III recall information in its January 16, 2002 Enforcement Report. A Class III recall is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences:

Recalls & Warnings

1/13/2019

Sexual Enhancement Supplement Recalled

On January 8, 2019, Happy Together, Inc. issued a recall of the sexual enhancement supplement Rhino 5k because FDA analysis found it to contain undeclared sildenafil and tadalafil.

Recalls & Warnings

9/25/2018

Seller of B Vitamins, Multis, Glucosamine & More Warned for Manufacturing Violations

On August 31, 2018, the FDA issued a warning letter to Independent Nutrition Inc., following a facility inspection which the company's products, including  B-50 Complete, Multi-Vitamin & Mineral Complex (a.k.a.

Recalls & Warnings

9/25/2018

FDA Warns Seller of Digestive Enzyme Supplements

On March 6, 2018, the FDA issued a warning letter to Uckele Health & Nutrition, Inc.

Recalls & Warnings

6/29/2018

Prescript-Assist Probiotic Recalled

On June 29, 2018, LL's Magnetic Clay, Inc., issued a recall of certain lots of Prescript-Assist, a "broad spectrum probiotic and prebiotic" supplement, because they may contain undeclared almonds, crustaceans, dairy, casein, eggs, and peanuts. 

Recalls & Warnings

2/27/2018

Testosterone, Thyroid, Other Supplements Recalled Due to Undeclared Milk

On February 23, 2018, Progressive Laboratories, Inc., issued a recall of the following four supplements because they may contain undeclared milk:

Recalls & Warnings

7/06/2018

Prescript-Assist Probiotic Recall Expanded

On July 6, 2018, LL's Magnetic Clay, Inc., expanded its original recall of Prescript-Assist, a "broad spectrum probiotic and prebiotic" supplement, because it may contain undeclared almonds, crustaceans, dairy, casein, eggs, and peanuts.

Recalls & Warnings

5/12/2018

Seller of Maca Powder Warned for Drug Claims

On April 18, 2018, the FDA issued a warning letter to Herbs America, Inc. following review of the company's website, and the company's Maca Magic store on www.amazon.

Recalls & Warnings

4/14/2018

Men's Sexual Enhancement Supplement Recalled

On April 12, 2018, AMA Wholesale Inc. recalled its sexual enhancement supplement Rhino 69 Extreme 50000 because it was found to contain undeclared tadalafil.

Recalls & Warnings

12/11/2020

Goldenseal Recalled Due to Microbial Contamination

On December 4, 2020, WishGarden Herbs, Inc. issued a recall of 14 lots of Cord Care Powder and Goldenseal Powder because they were manufactured using ingredients that were potentially contaminated with the bacterium Cronobacter sakazakii.

Recalls & Warnings

2/26/2020

Company Failed to Report Adverse Events Associated With Its Nutrition Shakes

On February 12, 2020, the FDA sent a warning letter to Market America Inc for failure to submit serious adverse event reports about two of its products, as required by federal regulation. The company received two reports following serious adverse events but did not submit the proper forms:

Recalls & Warnings

2/11/2020

FTC Sues Two Companies Selling Bone Health and Joint Pain Supplements

On February 11, 2020, the Federal Trade Commission (FTC) announced that it sued two companies to stop them from continuing to make false claims about their bone and joint health products, Ostinol (ZyCal Bioceuticals) and StimTein (Excellent Marketing Results, Inc. (EMR)).

Recalls & Warnings

6/23/2020

Seller of CBD Tinctures and "Immune Boost Packs" Warned for Coronavirus Claims

On June 18, 2020, the FDA issued a warning letter to Project 1600 Inc. for selling CBD products with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

6/25/2020

"Anti-Viral" Supplement Recalled for Unsupported Coronavirus Claims

On June 23, 2020, Golden Nutrition Inc. issued a recall of four lots of Anti-Viral Immune Enhancement Capsules because the label makes unsupported health claims to "help fight corona virus and influenza.

Recalls & Warnings

5/12/2020

Plum Dragon Herbs Warned for Coronavirus Claims

On May 8, 2020, the FDA issued a warning letter to Plum Dragon Herbs, Inc. for selling Chinese medicine products with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

3/09/2020

FDA Warns Sellers of Essential Oils, Colloidal Silver & Teas Promoted to Treat Coronavirus

On March 9, 2020, the FDA and FTC announced they have issued joint warning letters to seven companies for selling products such as essential oils, teas and colloidal silver with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

5/09/2020

FDA Warns Sellers of Essential Oils, CBD, Vitamins, and More Promoted to Treat Coronavirus

Between May 7 and May 8, 2020, the FDA issued warning letters to seven companies for selling products such as essential oils, CBD, hand sanitizers, and vitamins with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

3/31/2020

Bulletproof Warned for Manufacturing Violations

On March 20, 2020, the FDA issued a warning letter to Bulletproof 360, Inc.

Recalls & Warnings

3/24/2020

Mislabeled Lindt Chocolate Bar Recalled

On March 19, 2020, Lindt & Sprüngli (USA) Inc. issued a recall of one lot of Lindt Excellence 85% Cocoa chocolate bars because they are wrapped in the wrong packaging.

Recalls & Warnings

7/31/2020

FTC Sues Golden Sunrise for Marketing Deceptive $23,000 Coronavirus Cure

On July 31, 2020, the Federal Trade Commission (FTC) charged Golden Sunrise Nutraceutical, Inc., a California-based company, with deceptively advertising a $23,000 treatment plan as a scientifically proven way to treat COVID-19.

Recalls & Warnings

7/17/2020

Two More Hand Sanitizers That May Contain Toxic Ingredient Recalled

Update: (8/10/20) Soluciones Cosméticas has recalled additional products that may contain methanol, as listed in red below.

Recalls & Warnings

7/10/2020

FTC Charges Seller With Falsely Promising Consumers Next Day Shipping of Face Masks and Other PPE

On July 8, 2020, the Federal Trade Commission (FTC) charged the online marketer SuperGoodDeals.com, Inc. and its owner, Kevin J. Lipsitz, with falsely promising consumers next-day shipping of facemasks and other personal protective equipment (PPE) to use during the coronavirus pandemic.

Recalls & Warnings

7/07/2020

Seller of Homeopathic Products Warned for Manufacturing Violations

On June 19, 2020, the FDA issued a warning letter to Washington Homeopathic Products, Inc.

Recalls & Warnings

9/01/2020

Harmonic Nature Hand Sanitizer Recalled

On August 28, 2020, Harmonic Nature recalled their hand sanitizer because it may contain 1-propanol, which is toxic when ingested.

Recalls & Warnings

4/24/2021

Metal Reported in Church & Dwight Gummy Melatonin, Multis & Fiber Supplements

On April 20, 2021, Church & Dwight Co., Inc.

Recalls & Warnings

3/18/2021

Don't Drink Real Water Alkaline Water, FDA Warns After Reports of Liver Illness

On March 16, 2021, the FDA warned consumers not to drink or use Real Water bottled alkaline water while it investigates reports of hepatitis associated with the product.

Recalls & Warnings

1/04/2007

Sellers of Popular Weight Loss Supplements Pay $25 Million Over FTC Allegations of Deceptive Advertising

On January 4, 2007, the Federal Trade Commission (FTC) announced that it had filed complaints in four separate cases alleging that weight-loss and weight-control claims were not supported by competent and reliable scientific evidence.

Recalls & Warnings

9/23/2005

FTC Continues Litigation Against Makers of CortiSlim and CortiStress Supplements

On September 21, 2005 the Federal Trade Commission (FTC) announced that three defendants will give up $4.

Recalls & Warnings

5/28/2003

FTC Challenges Claims of Five Supplements to Treat or Cure Serious Diseases

On May 27, 2003 the Federal Trade Commission announced that it had filed a complaint in federal district court against A.

Recalls & Warnings

9/15/2005

Weight Loss Pill Marketer in Settlement with New Jersey Attorney General

On August 16, 2005, New Jersey Attorney General Peter C. Harvey and Consumer Affairs Director, Kimberly Ricketts, announced that Goen Technologies Corp.

Recalls & Warnings

7/11/2017

Gluten Free Chocolate Chip Bars Recalled Due to Allergen Risk

On July 10, 2017, Coborn's, Inc. recalled packages of Gluten Free Chocolate Chip Bars because some were incorrectly labeled as Gluten Free Fudge Brownies.

Recalls & Warnings

7/04/2017

FDA Warns Against Company's Unsafe Teething Tablets

On June 20, 2017, the FDA issued a warning letter to Raritan Pharmaceuticals, Inc. following a routine inspection of the facility when it found the company's Homeopathic Infant's Teething Tablets in violation of current good manufacturing practice (CGMP) regulations.

Recalls & Warnings

7/18/2017

Oat Cereal Recalled Due to Listeria Risk

On July 18, 2017, Garden of Light, Inc., recalled Woodstock Organic Matcha Vanilla Oats because of potential contamination with Listeria monocytogenes.

Recalls & Warnings

11/22/2017

FDA Warns Distributor of "Testosterone Wellness for Men"

On November 8, 2017, the FDA sent a warning letter to Vita-Pure, Inc.

Recalls & Warnings

9/23/2017

Enhancement Supplement "Vegetable Vigra" Recalled

On September 20, 2017, Gadget Island, Inc. Dba Gear Isle recalled VEGETABLE VIGRA [sic] after FDA testing found undeclared presence of sildenafil. 

Recalls & Warnings

1/24/2020

Fat-Burning, Energy Supplement Linked to Heart Trouble

A 33-year-old woman in Australia developed cardiac ischemia (a lack of blood flow to the heart) after taking the "fat burning" supplement Alpha Lean-7, according to a recent report in the Journal of Sports Sciences.

Recalls & Warnings

10/08/2019

Seller of Tea, Colloidal Silver, Homeopathic Products Warned for Manufacturing Violations

On September 12, 2019, the FDA issued a warning letter to Herbal Healer Academy, Inc.

Recalls & Warnings

10/01/2019

Lead and Arsenic Found in Multi Mineral & Vitamin Supplement

On September 30, 2019, Cellect Products Inc. and Oglethorpe Ltd. issued a recall of one lot of Cellect®, Essentials Factor® Multi Mineral & Vitamin Supplement Unflavored Powder Mix because it was found to contain unsafe levels of lead and arsenic.

Recalls & Warnings

9/21/2019

Liquid Vitamin C for Men Recalled

On September 16, 2019, Fitoterapia USA Inc. issued a recall of Macho Artificial Passion Fruit Flavored Vitamin C Liquid Supplement, a supplement promoted for male sexual enhancement, because FDA analysis found it to contain tadalafil.

Recalls & Warnings

11/29/2019

FDA Warns Seller of "All Natural" Treatment for Opioid Withdrawal, Migraines & More

On November 18, 2019, the FDA issued a warning letter to EPH Technologies, Inc., following a review of the company's websites, which found statements made about some of the company's products, including Detoxoplex, Sinople, and Migrenz, to be drug claims.

Recalls & Warnings

7/23/2019

FDA Warns Seller of CBD Lotions, Patches, Tinctures and Pet Products

On July 22, 2019, the FDA issued a warning letter to Curaleaf, Inc.

Recalls & Warnings

7/16/2019

FDA Warns Seller of Magnesium and CBD

On July 9, 2019, the FDA issued a warning letter to Ceba-Tek, Inc.

Recalls & Warnings

6/16/2019

"Immune Support" Throat Sprays Recalled

On June 13 2019, APS BioGroup, Inc. issued a recall of four "immune support" throat sprays because they have the potential to be contaminated with Stenotrophomonas maltophilia, a bacteria that can cause respiratory infection, particularly in individuals with weakened immune systems.

Recalls & Warnings

5/25/2019

Department of Justice Files Complaint to Shut Down Supplement Company

On May 23, 2019, the United States Department of Justice announced a complaint seeking a permanent injunction has been filed against dietary supplement marketers Helen Chian and Jim Chao, president and company manager of Confidence USA Inc.

Recalls & Warnings

4/02/2019

FDA Issues Strong Warnings to Sellers of CBD

On March 28, 2019, the FDA issued warning letters to three companies for making unsubstantiated claims about the health benefits of CBD (cannabidiol) products on their websites.

Recalls & Warnings

3/26/2019

Seller of NeuSilver Colloidal Silver for Adults, Children and Pets Warned by FDA

On February 19, 2019, the FDA issued a warning letter to iMedDo, Inc., following a review of the company's website, http://www.imeddo.

Recalls & Warnings

3/23/2019

BLUEFUSION Capsules for Sexual Enhancement Recalled

On March 21, 2019, Ata Int. Inc. issued a recall of its BLUEFUSION capsules, which are promoted for sexual enhancement, because FDA analysis found them to contain sildenafil, tadalafil, desmethyl carbodenafil, dithiodesmethyl carbodenafil, scutellarin and daidzein.

Recalls & Warnings

6/04/2020

FTC Warns 35 More Companies for Coronavirus Claims

On June 4, 2020, the FTC announced that it sent warning letters to 35 companies for selling products such as herbal products, immune system boosters, and vitamin C with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

7/13/2005

Recall of Multivitamins with Iron Lacking Child-Resistant Caps

On July 12, 2005, The U.S. Consumer Product Safety Commission in cooperation with NBTY, Inc. announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Recalls & Warnings

5/29/2003

Recall and Warning for Another Sexual Enhancement Supplement Illegally Containing Viagra Ingredient

On May 23, Best Life International, in cooperation with the U.S. Food and Drug Administration, warned consumers not to purchase or consume the product known as Viga.

Recalls & Warnings

11/18/2003

Supplement Promoted As Cancer Treatment Removed from Market

On November 10, 2003, the Food and Drug Administration (FDA) announced that NBTY, Inc., of Bohemia, N.Y.

Recalls & Warnings

7/24/2006

Marketers of Seasilver Ordered to Pay Almost $120 Million

On July 24, 2006, the Federal Trade Commission (FTC) announced that the marketers of Seasilver, an alleged phony cure-all, have been ordered to pay almost $120 million for failing to comply with an earlier order requiring them to pay $3 million in consumer redress.

Recalls & Warnings

3/20/2007

Recall of Adulterated Sexual Enhancement Supplement

As posted on the FDA website, on March 15, 2007, the company Barodon SF of Los Angeles, CA announced that it is conducting a voluntary nationwide recall of the company's supplement product sold under the name V.MAX.

Recalls & Warnings

4/22/2008

Court Upholds Order for Seasilver Marketers to Pay $120 Million

On April 16, 2008, the Federal Trade Commission (FTC) announced that the U.S.

Recalls & Warnings

3/06/2009

"The Truth About Nutrition" Marketers Agree to Pay $3 Million to Settle Charges of Deceptive Advertising of Dietary Supplements and Devices

On March 6, 2008, the Federal Trade Commission (FTC) announced that marketers of dietary supplements and health-related devices have agreed to pay $3 million in consumer redress to settle FTC charges that they deceptively claimed their products treated or prevented a wide variety of serious ...

Recalls & Warnings

12/20/2011

Organic Celery Seed Products Recalled Due to Potential Salmonella Contamination

On December 16, 2011, the U.S. FDA posted a notice from Swanson Health Products regarding the recall of Swanson Organic Celery Seed (Whole) which is packaged in plastic bottles with a net weight of 1.4 oz. (40 grams) because it has the potential to be contaminated with Salmonella.

Recalls & Warnings

11/27/2011

FDA Seeks Permanent Injunction Against Dietary Supplement Maker -- 400+ Products Affected

On November 23, 2011, the U.S. FDA took legal action against a dietary supplement maker and owner for substituting ingredients and products without noting the changes on the final product labels. The permanent injunction, filed on behalf of the FDA by the U.S.

Recalls & Warnings

12/26/2010

Four Probiotic Products in Canada May Pose Serious Health Risks to Those with Milk or Soy Allergies

On December 24, 2010, Health Canada (the Canadian health ministry) advised consumers with milk or soy allergies that four probiotic natural health products are being voluntarily recalled from the market because they are labelled as not containing dairy (milk) and/or soy but may contain trace ...

Recalls & Warnings

9/15/2010

Recall of Testosterone-Boosting Supplement

On September 14, 2010, the FDA posted a notice that KiloSports is recalling Clomed (60 count bottles), a supplement with claims to "release gonadatropin," "elevate testosterone" and "promote spermatogenesis."

Recalls & Warnings

12/02/2014

Glucosamine Class-Action Settlement Reversed by Appeals Court

On November 19, 2014, an appeals court rejected a settlement of a class-action lawsuit that alleged label claims on glucosamine products manufactured or sold by Rexall Sundown, Inc., NBTY, Inc. or their affiliates, were false, deceptive or misleading.

Recalls & Warnings

9/16/2015

Weight And Enhancement Supplement Recall Expanded

On September 11, 2015, One Minute Miracle Inc. issued a recall of all lots the following supplements which were found to contain undeclared drugs:

Recalls & Warnings

9/05/2015

Powdered Caffeine Risky, FDA Warns

On August 27, 2015, the FDA issued a warning letter to five companies selling caffeine powder, warning that the powder "presents a significant or unreasonable risk of illness or injury under the conditions of use recommended or suggested in the labeling."

Recalls & Warnings

4/11/2015

Acai Berry Marketers Who Tricked Consumers with Fake News Sites Ordered to Pay $16 Million

On April 6, 2015, the Federal Trade Commission (FTC) announced that a recent U.S. district court ruling will require marketing affiliates for LeanSpa's acai berry and "colon cleanse" weight loss products to pay $16 million in consumer redress.

Recalls & Warnings

2/06/2013

Ingredient Supplier Warned For Meal Replacement Product Misbranding and Adulteration

On October 4, 2012, the FDA issued a warning letter to dietary supplement ingredient supplier Raw Deal, Inc.

Recalls & Warnings

3/02/2013

FDA Finds Manufacturing Violations At NSF-Certified Supplement Facility

The FDA recently warned dietary supplement manufacturer Beehive Botanicals, Inc.

Recalls & Warnings

1/04/2014

Beware of Supplements Claiming to Treat Brain Injury, FDA Warns

On December 31, 2013, the FDA warned consumers to avoid dietary supplements promoted to prevent, treat or cure concussions and other traumatic brain injuries (TBIs).

Recalls & Warnings

6/20/2013

Glucosamine Legal Settlement Over Labeling -- Many Products Covered

On May 16, 2013, a U.S. District Court preliminarily approved a settlement of class action cases alleging that certain claims made on the labeling of specific glucosamine products are false, deceptive, and misleading. No allegations related to safety or physical injury have been made.

Recalls & Warnings

4/06/2018

Workout Supplements Recalled Due To Allergen Risk

On April 5, 2018, Independent Nutrition Inc, dba Back to Health of Eugene., issued a recall of certain lots of Ignite High Endurance Pre-Workout Supplements because they may contain undeclared milk.

Recalls & Warnings

7/03/2018

FDA Warns Seller of Adulterated Chinese Herbal Supplements

On June 20, 2018, the FDA issued a warning letter to KPC Products, Inc.

Recalls & Warnings

2/17/2018

FDA Warns Seller Reishi Mushroom Supplements

On February 7, 2018, the FDA issued a warning letter to Reishi D. International, Inc., following a facility inspection which found the company's Reishi D.

Recalls & Warnings

3/16/2018

FTC Sends Refund Checks to Consumers of Unproven Weight-Loss Products

On March 15, 2018, the FTC announced it is mailing 18,301 checks totaling more than $437,000 to consumers who purchased weight-loss products from Colby Fox, Christopher Reinhold, and their companies, Tachht, Inc. and Teqqi, LLC.

Recalls & Warnings

6/19/2018

FDA Warns Seller of Weight Control Patches

On June 6, 2018, the FDA issued a warning letter to Health Management Group, Inc.

Recalls & Warnings

6/05/2018

FDA Warns Seller of Colloidal Silver

On May 17, 2018, the FDA issued a warning letter to Silver Armor, Inc.

Recalls & Warnings

5/22/2018

FDA Warns Companies Selling "Sun Protection" Supplements

On May 18, 2018, the FDA issued warning letters to four companies selling supplements for sun protection because statements made on product labels, websites and in marketing materials were found to be drug claims, which are not permitted for dietary supplements. 

Recalls & Warnings

5/19/2018

Homeopathic Teething Drops, Nausea Drops, Silver-Zinc Throat Spray & More Recalled

On May 18, 2018, MBI Distributing, Inc.

Recalls & Warnings

5/19/2018

Sexual Enhancement Supplements Containing Undeclared Drugs Recalled

On May 17, 2018, Shoreside Enterprises, Inc., recalled certain lots of its sexual enhancement supplements 7K and Poseidon 4500 (Extreme 1000 mg) because they were found to contain undeclared sildenafil and/or tadalafil.

Recalls & Warnings

5/15/2018

Seller of Apple Cider Vinegar, Joint Supplements & More Warned for Drug Claims

On April 25, 2018, the FDA issued a warning letter to Baker's Best Health Products, Inc.

Recalls & Warnings

9/22/2018

MyoWhey Protein Powder Recalled

On September 20, 2018, Purus Labs, Inc. issued a recall of one lot of MyoWhey Chocolate Cookie Crunch protein powder because it may contain undeclared milk and soy.

Recalls & Warnings

9/19/2018

Seller of Curcumin, Garcinia, Glucosamine and More Warned for Manufacturing Violations

On September 7, 2018, the FDA issued a warning letter to Best Nutrition Products, Inc.

Recalls & Warnings

12/12/2018

Seller of Protein Powder, Spirulina & Other Products Warned for Manufacturing Violations

On October 31, 2018, the FDA issued a warning letter to DynaPro International, Inc.

Recalls & Warnings

12/01/2018

Seller of 5-HTP, Potassium & More Warned for Manufacturing Violations

On September 7, 2018, the FDA issued a warning letter to The Delano Company, Inc.

Recalls & Warnings

11/27/2018

More Dog Food Recalled Due to Risk of Vitamin D Toxicity

On November 27, 2018, Sunshine Mills, Inc. issued a recall of select Evolve Puppy, Sportsman's Pride Large Breed Puppy and Triumph Chicken and Rice Dog Food because they may contain elevated levels of vitamin D.

Recalls & Warnings

9/01/2018

Homeopathic Remedies Contaminated With Bacteria

On August 29, 2018, Hellolife, Inc.

Recalls & Warnings

8/20/2019

Seller of Liposomal Curcumin, Vitamin C & Melatonin Warned for Manufacturing Violations

On August 6, 2019, the FDA issued a warning letter to Let's Talk Health, Inc.

Recalls & Warnings

1/23/2020

Flaxseed Salmonella Risk Prompts Recall

Update: (2/4/20) This recall has been expanded to include additional Nopalina flaxseed products, which are highlighted below.

Recalls & Warnings

8/01/2013

Fat Loss and Muscle Enhancement Supplements Found To Contain DMAA

On June 17, 2013, the FDA issued a warning letter to Formulife, Inc., dba Purus Labs, Inc., following a facility inspection which found the dietary supplements Fat Smack XR Thermolipolytic, Muscle Marinade Fresh Fruit and Muscle Marinade Cherry Limeade to contain DMAA.

Recalls & Warnings

4/04/2013

Three More Sexual Enhancement Supplements Found To Contain Undeclared Drugs

On April 3, 2013, the FDA warned consumers that the sexual enhancement supplements AFFIRM XL, Love Rider and Ninja Mojo were found to contain undeclared erectile dysfunction drugs. Consumers are urged to stop using these supplements immediately.

Recalls & Warnings

3/29/2013

Prescription Drugs Found In Prostate and Sexual Enhancement Supplements

October 24, 2012 the FDA issued a warning letter to USA Far Ocean Group Inc./ Health & Beauty Group Inc. because a number of the company's dietary supplements were found to contain pharmaceutical drugs, or were promoted with statements that constitute drug claims.

Recalls & Warnings

12/21/2012

FDA Warns Maker of Glucosamine and Omega-3 Supplements For Manufacturing Violations

On December 7, 2012, the FDA issued a warning letter to Basic Organics, Inc. following a facility inspection which found the company's Glucosamine Chondroitin and Omega 3 dietary supplements to be adulterated.

Recalls & Warnings

10/24/2012

FDA Seizes Many Supplements from New York Company Due To Drug Claims

On October 23, 2012, U.S. Marshalls, acting on behalf of the FDA, seized dietary supplements and unapproved drugs from Confidence, Inc., a supplement manufacturer in Port Washington, N.Y. The products included dietary supplements Dr.

Recalls & Warnings

8/30/2015

Weight and Enhancement Supplements Recalled

On August 27, 2015, One Minute Miracle Inc. issued a recall of one lot each the following supplements which were found to contain undeclared drugs:

Recalls & Warnings

7/15/2010

Supplement Company Pays $5.5 Million to Settle False Advertising Claims

On July 14, 2010, the Federal Trade Commission (FTC), as part of its ongoing efforts to stop bogus health claims, announced that it is requiring a major marketer of dietary supplements to pay $5.

Recalls & Warnings

10/26/2011

FDA Warns Supplement Maker of Manufacturing Violations Affecting Many Products

The U.S. FDA has sent a Warning Letter (dated 10/17/2011) to Health Advances USA, Inc. regarding manufacturing violations that cause its dietary supplement products to be considered adulterated.

Recalls & Warnings

6/21/2011

FDA Seizes Probiotics Over Marketing Claims

On June 7, 2011, the U.S. FDA announced that, at its request, U.S. Marshals seized probiotic products from UAS Laboratories, Inc., of Eden Prairie, Minn. because the company markets the products as drugs.

Recalls & Warnings

1/10/2012

Acai Berry Pill Marketers to Pay $1.5 Million to Settle FTC Charges

On January 9, 2012, the U.S. Federal Trade Commission (FTC) announced that an operation that marketed acai berry supplements, "colon cleansers," and other products using allegedly fraudulent free trial offers and phony endorsements from Oprah Winfrey and Rachael Ray will pay $1.

Recalls & Warnings

1/02/2012

FDA Warns XYMOGEN of Manufacturing and Labeling Violations Regarding Multiple Products

On December 13, 2011, the U.S. FDA sent a Warning Letter to Atlantic Pro Nutrients, Inc. (dba XYMOGEN) regarding labeling and/or manufacturing violations relating to its products, which include Borage CP-240, CoQmax CF, Immune Rx, Iron Glycinate, and Green Tea 600.

Recalls & Warnings

5/01/2009

FDA Warns Consumers to Stop Using Hydroxycut -- Product Being Tested by ConsumerLab.com

On May 1, 2009, the U.S. Food and Drug Administration warned consumers to immediately stop using Hydroxycut products by Iovate Health Sciences Inc., of Oakville, Ontario and distributed by Iovate Health Sciences USA Inc. of Blasdell, N.Y.

Recalls & Warnings

3/02/2005

Marketer of Weight-Loss System Settles FTC Charges of Deceptive Advertising

On March 1, 2005, the Federal Trade Commission (FTC) announced that California infomercial producer Modern Interactive Technology, Inc.

Recalls & Warnings

10/06/2004

False Claims Made by Marketer of Cortisol-related Weight-Loss Supplements According to FTC

On October 6, 2004, the Federal Trade Commission (FTC)charged marketers of two dietary supplements with claiming, falsely and without substantiation, that their products can cause weight loss and reduce the risk of, or prevent, serious health conditions.

Recalls & Warnings

10/25/2016

Seller of Liquid Aloe & Mineral Supplement Warned for Manufacturing Violations

On August 10, 2016, the FDA issued a warning letter to Perfect Source Natural Products Inc.

Recalls & Warnings

3/08/2016

Maker of Calcium and Vitamin C Supplements Warned for Manufacturing Violations

On September 17, 2015, the FDA issued a warning letter to Raphah, Inc.

Recalls & Warnings

6/18/2016

Antioxidant Supplement Recalled Due to Allergen Risk

On June 17, 2016 GMJ Natural Products Inc. issued a recall of 32 fluid oz. jugs of Jugo Moringa Plus Antioxidant because they contain undeclared whey protein.

Recalls & Warnings

5/23/2016

Amino Acid Supplements Recalled

On May 18, 2016, Ultimate Nutrition Inc. issued a recall of its Amino Gold amino acid tablets and capsules because they contain undeclared milk in the form of hydrolyzed whey protein.

Recalls & Warnings

9/21/2017

Sexual Enhancement Supplements Containing Prescription Drugs Recalled

On September 20, 2017, Gadget Island, Inc. Dba Gear Isle recalled the following supplements because they were found to contain undeclared sildenafil and tadalafil:

  • Rhino 7 Platinum 5000 capsules, Lot# R7-D5K1011H

Recalls & Warnings

8/29/2017

FDA Warns Seller of Supplements for Allergies, Joint Pain, Bone Health, and More

On August 16, 2017, the FDA issued a warning letter to Total Nutrition, Inc.

Recalls & Warnings

7/24/2017

Protein Bars Recalled Due to Listeria Risk

On July 21, 2017, Bhu Foods recalled a number of their products after their organic sunflower seeds, distributed by Hudson Valley Foods, Inc., were potentially contaminated with Listeria monoocytogenes.

Recalls & Warnings

1/30/2018

Limbrel for Osteoarthritis Recalled Due to Risk of Adverse Effects

On January 26, 2018, Primus Pharmaceuticals, Inc. of Scottsdale, Arizona issued a recall of all unexpired lots of Limbrel products.

Recalls & Warnings

1/29/2018

Seller of Male Enhancement, Prostate Supplements & More Warned for Drug Claims

On January 10, 2018, the FDA issues a warning letter to USA Labs AKA Power Source Distributors, Inc following a review of the company's website which found statements made about its products, including Maximum Male, Beta 300 (Beta Prosturol), Chromium Max 1000, DHEA, Healthy Cold-X and ...

Recalls & Warnings

1/26/2018

Seller of Coenzyme-A Warned For Making Drug Claims

On January 5, 2018, the FDA issued a warning letter to Coenzyme A, Inc. following a facility inspection and review of the company's website that found the company made drug claims about its product Coenzyme-A.

Recalls & Warnings

1/25/2018

Bulletproof Collagen Protein Recalled

On January 25, 2018, Bulletproof 360, Inc issued a recall of its Bulletproof Collagen Protein supplement because it contains undeclared milk.

Recalls & Warnings

12/26/2017

Seller of Fish Oil, Vitamin D, Whey Protein and More Warned for Manufacturing Violations

On December 19, 2017, the FDA issued a warning letter to Maine Natural Health, Inc.

Recalls & Warnings

12/23/2017

Seller of Meal Replacement, Protein Drinks, Cranberry and More Warned for Manufacturing Violations

On July 6, 2017, the FDA issued a warning letter to Professional Botanicals, Inc.

Recalls & Warnings

4/19/2017

Sexual Enhancement Supplements for Men and Women Recalled

On April 18, 2017, Organic Herbal Supply, Inc. issued a recall of all lots of the following sexual enhancement supplements for men because they were found to contain the undeclared drug tadalafil:

Recalls & Warnings

4/04/2017

Seller of B Vitamins, Vitamin C, Potassium & More Warned for Manufacturing Violations

On March 24, 2017 the FDA issued a warning letter to The Sanapac Company, Inc.

Recalls & Warnings

3/21/2017

Twenty-one Sexual Enhancement Products Recalled

On March 7, 2017, A&H Focal Inc. issued a recall of the following sexual enhancement supplements because they were found to contain drugs such as sildenafil, tadalafil, vardenafil:

Recalls & Warnings

2/21/2017

Sexual Enhancement Supplement Recalled

On February 16, 2017, Organic Herbal Supply, Inc. issued a recall of its sexual enhancement supplement XtraHRD Natural Male Enhancement because it was found to contain tadalafil.

Recalls & Warnings

2/16/2017

U.S. Department of Justice Files Permanent Injunction Against Supplement Manufacturer

On February 16, 2017, the United States Department of Justice filed a complaint against Pick and Pay, Inc.

Recalls & Warnings

2/14/2017

Life Extension Warned for Drug Claims

On February 1, 2017, the FDA issued a warning letter to Life Extension Foundation Buyers Club, Inc.

Recalls & Warnings

2/09/2017

Herbal Supplement Found to Contain Ephedra Alkaloids Recalled

On February 7, 2017, Kingsway Trading Inc. issued a recall of Xanthium & Siler Combo (Bi Yan Pian) Dietary Supplement because it contains ephedra alkaloids.

Recalls & Warnings

2/09/2017

Federal Court Orders Dietary Supplement Distributor to Stop Selling Its Products

On February 9, 2017, the FDA announced that VivaCeuticals Inc, doing business as Regeneca Worldwide, has been ordered by a federal court to stop selling its products, which were found to contain unsafe ingredients including DMAA.

Recalls & Warnings

2/07/2017

Seller of Chinese Herbal Products for Prostate, Menopause and More Warned for Manufacturing Violations

On January 23, 2017, the FDA issued a warning letter to Herbal Sciences International, Inc.

Recalls & Warnings

11/12/2017

Weight Loss and Cleanse Supplements Contain Adulterated and Improperly Labeled Ingredients, FDA Warns

On November 2, 2017, the FDA issued a warning letter to Create-A-Pack Foods, Inc.

Recalls & Warnings

10/18/2017

FDA Warns Seller of Arthritis, Blood Pressure, Diabetes Supplements For Making Drug Claims

On August 15, 2017, the FDA issued a warning letter to Years to Your Health, Inc., following an inspection of the company's website which found a number of their products to be misbranded, as they contained drug claims.

Recalls & Warnings

10/17/2017

Organic Tarragon Spice Recalled Due to Salmonella Risk

On October 16, 2017, Organic Spices, Inc. dba Spicely Organics issued a recall of its Organic Tarragon because it has the potential to be contaminated with Salmonella.

Recalls & Warnings

10/13/2017

Hi-Tech To Pay Over 40 Million to Settle FTC Charges of False Claims

On October 11, 2017, a U.S. District Judge ruled that Hi-Tech Pharmaceuticals Inc.

Recalls & Warnings

9/28/2017

Seller of Prostate, Reishi Supplements Warned for Manufacturing Violations

On September 11, 2017, the FDA issued a warning letter to Vicare International (USA), Inc.

Recalls & Warnings

9/26/2017

FDA Warns Seller of DHEA, Creatine, Chromium & More for Manufacturing Violations, Drug Claims

On August 25, 2017, the FDA issued a warning letter to Mega-Pro Nutrition, Inc., following inspections of the facility and website www.mega-pro.

Recalls & Warnings

7/18/2017

FDA Warns Seller of "Quick Slim with pure Hoodia Gardonii" and "Diabalance Herbal Blood Sugar Balance"

On July 11, 2017, the FDA issued a warning letter to Black Seed Herb, Inc.

Recalls & Warnings

7/11/2017

FDA Warns Dr. Carolyn Dean of Drug Claims Made for Magnesium, Calcium & Other Mineral Supplements

On June 27, 2017, the FDA issued a Warning Letter to Dr. Carolyn Dean of New Capstone, Inc.

Recalls & Warnings

6/27/2017

Seller of Alpha Lipoic Acid, Cinnamon Supplements and More Warned For Manufacturing Violations

On May 1, 2017 the FDA issued a warning letter to Nature's Vision, Inc.

Recalls & Warnings

6/17/2017

Protein Bars and Bites Recalled Due to Listeria Risk

On June 15, 2017, Bulletproof 360, Inc. recalled five Collagen Protein Bar and Bite products because of potential contamination with Listeria monocytogenes.

Recalls & Warnings

6/10/2017

Seller of Prostate, Immune Supplements & More Warned for Manufacturing Violations

On May 25, 2017 the FDA issued a warning letter to The Herbalist, Inc.

Recalls & Warnings

5/30/2017

Maker of Collagen Supplement Warned for Manufacturing Violations

On July 17, 2014, the FDA issued a warning letter to Morhaim Pharmalab, Inc.

Recalls & Warnings

5/02/2017

Seller of Amino Acid Supplements & More Warned for Manufacturing Violations

On April 20, 2017 the FDA issued a warning letter to Naturecom Inc.

Recalls & Warnings

9/12/2018

FDA Urges Consumers to Avoid Kratom

On September 11, 2018, FDA Commissioner Scott Gottlieb, M.D., urged consumers not to use products containing the kratom, an herb that is often promoted for pain relief and for relieving symptoms of opioid withdrawal.

Recalls & Warnings

9/08/2018

Homeopathic Oral Sprays Recalled Due to Possible Bacterial Contamination

On September 5, 2018, Beaumont Bio Med, Inc., issued a recall of all of its water and alcohol-based homeopathic products because they have the potential to contain microbial contaminants. 

Recalls & Warnings

3/17/2004

Marketers of “Focus Factor” and “V-Factor” Fined for Advertising Claims

On March 17 , 2004 the Federal Trade Commission (FTC) reported that the marketers of “Focus Factor,” a dietary supplement that purports to improve concentration, and “V-Factor,” a supplement that purports to enhance sexual performance, have agreed to settle charges that they made numerous ...

Recalls & Warnings

3/09/2004

FTC Stops False Advertising by Makers of Weight Loss and Arthritis “Cures”

On March 9, 2004, the Federal Trade Commission (FTC) announced that several direct mail marketers have agreed to pay $2.

Recalls & Warnings

10/24/2003

Court Closes the Doors on Company That Sold Weight Loss Supplement

On October 24, 2003, the Federal Trade Commission (FTC)announced that Mark Nutritionals, Inc. and Edward D’Alessandro, Jr. have agreed to settle federal charges that they used false and unsubstantiated claims to sell their weight-loss product.

Recalls & Warnings

8/14/2008

Airborne to Pay $30 Million for Deceptive Advertising of Cold Remedy -- Refunds Available

On August 14, 2008, the Federal Trade Commission (FTC) announced that Airborne Health, Inc.

Recalls & Warnings

1/17/2006

FDA Warns Consumers about Brazilian Diet Pills Found to Contain Active Drug Ingredients

On January 13,2006, the U.S. Food and Drug Administration (FDA) warned consumers not to use two unapproved drug products that are being marketed as dietary supplements for weight loss.

Recalls & Warnings

8/18/2006

Restitution Program for Purchases of Lane Labs' Products

On August 17, 2006 the Food and Drug Administration (FDA) announced that it was notifying consumers of a restitution (refund) program for purchasers of three of Lane Labs-USA, Inc.'s products. The products are BeneFin, MGN-3 and SkinAnswer.

Recalls & Warnings

7/23/2009

Six Male Enhancement Supplements Found Adulterated

On July 15, 2009, the U.S. FDA announced that Obteron 1 Inc. dba Nature & Health Co. is recalling the following supplements: LibieXtreme, Y-4ever, Libimax X Liquid, Powermania Capsule, Powermania Liquid, and Herbal Disiac.

Recalls & Warnings

11/02/2008

Sales of Weight-Loss Supplement Suspended -- May Contain Diuretic Drug

On October 31, 2008, Associated Press reported that makers of the weight loss supplement StarCaps have suspended sales following accusations that the product contains a non-listed pharmaceutical diuretic, Bumetanide.

Recalls & Warnings

4/15/2003

FTC Requires Scientific Evidence for "Snore Formula" Claims

On April 15 2003, the U.S. Federal Trade Commission (FTC) announced that an Arizona-based company, Snore Formula, Inc., its officers, and a distributor have agreed to settle FTC charges that they failed to have scientific substantiation for the claims made for "Dr.

Recalls & Warnings

1/18/2003

Non-Prescription Anti-Hypertension Pills Recalled

On January 17, the U.S. FDA's MedWatch Program reported that Herbsland Inc.

Recalls & Warnings

12/11/2002

Recall of Calcium Supplement Possibly Contaminated with Antibiotic

The U.S. Food and Drug Administration (FDA) released the following Class II recall information in its December 11, 2002 Enforcement Report.

Recalls & Warnings

6/09/2005

FTC Cracks Down on "HGH" Supplements; $20 Million in Consumer Redress

On June 9, 2005, The Federal Trade Commission (FTC) announced that two Florida businesses have agreed to a federal court order requiring them to pay up to $20 million in consumer redress – the largest monetary judgment ever obtained in an FTC health fraud case – to settle charges that they ...

Recalls & Warnings

1/31/2012

FTC Stops Fake News Sites About Acai Berry Products

As published on the U.S. Federal Trade Commission's (FTC) website on January 25, 2011, six online marketers settled with the FTC to stop posting fake news on websites intended to promote acai berry supplements and other weight-loss products.

Recalls & Warnings

3/03/2012

FDA Warns Vitaganic of Manufacturing Violations

On February 8, 2012, the U.S. FDA sent a Warning Letter to Vitaganic, Inc. regarding violations of Current Good Manufacturing Practic (CGMP) regulations for dietary supplements found during an inspection of it manufacturing facility in Sunnyvale, California in October 2011.

Recalls & Warnings

5/13/2012

Caffeinated Water Illegally Promoted According to FDA

On April 24, 2012, the U.S. FDA sent a Warning Letter to Vitality Distributing, Inc. indicating that the company's product "avitae caffeinated water" is being illegally promoted as an unapproved new drug due to claims relating to its safety and efficacy, such as the following:

Recalls & Warnings

6/13/2012

Tart Cherry Supplement Selller Warned by FDA Over Illegal Health Claims

The U.S. FDA recently published a Warning Letter (dated June 8, 2012) to Michelle's Miracle, Inc. for illegally promoting a range of tart cherry dietary supplements using health claims reserved for drugs. The products cited are: 

Recalls & Warnings

4/04/2012

Maker of Protein Drinks and Supplements Warned of Manufacturing Violations

The FDA published a Warning Letter to Protica, Inc., a maker of protein drinks and supplements, regarding violations of manufacturing regulations discovered during inspection of its facility in Whitehall, PA. Affected products include the foods Amped Up-2oz, Fireball-2oz, Healthy Shot-2.

Recalls & Warnings

3/14/2012

Manufacturing Violations by Maker of Lecithin, Soy Supplements

The FDA issued a Warning Letter (dated March 7, 2012) to Modern Products, Inc. regarding manufacturing violations in the production of the supplements Fearn Lecithin Granules, Fearn Liquid Lecithin, Fearn 100% Soy Protein Isolate, and Gayelord Hauser Brewers Yeast.

Recalls & Warnings

3/07/2012

Melatonin in Cookies and Drinks -- Not Allowed, Says FDA

On December 8, 2011 FDA issued a letter to Revolt Distribution, Inc. warning that their food and beverage products contain an unsafe food additive.

Recalls & Warnings

10/17/2012

Maker of Probiotic Supplement Warned for Manufacturing Violations

On September 28, 2012, the FDA issued a warning letter to dietary supplement manufacturer James G. Cole Inc.

Recalls & Warnings

9/10/2012

Maker of Concussion Recovery Supplement Warned For Making Drug Claims

On August 28, 2012, the FDA issued a warning letter to Trinity Sports Group, Inc. after a review of the company's websites found statements about Neuro Impact Concussion Response Formula constituted drug claims not permitted on supplements. 

Recalls & Warnings

9/08/2012

Medifast Settles False Advertising Suit

On September 7, 2012, Jason Pharmaceuticals Inc., a wholly owned subsidiary of Medifast, agreed to pay a $3.7 million civil penalty and meet new compliance requirements as part of a settlement with the U.S. Department of Justice and the Federal Trade Commission.

Recalls & Warnings

4/07/2011

Prostate Drug Found in Prostate Supplement -- Recall Underway

On March 24, 2011 the U.S. FDA posted a voluntary recall notice for U-Prosta from USA Far Ocean Group, Inc.

Recalls & Warnings

10/07/2011

Recall of Whey Protein Powders Due to Allergens

On October 6, 2010 the FDA posted a recall notice from Prolab Nutrition Inc. (dated September 30) indicating that some of its PROLAB protein powders are being recalled as they may contain undeclared milk, wheat and gluten allergens.

Recalls & Warnings

7/15/2014

Pinnacle Labs International Warned for Manufacturing Violations

On June 24, 2014, the FDA issued a warning letter to Pinnacle Labs International, Inc.

Recalls & Warnings

7/15/2014

Vita Springs Health Warned for Manufacturing Violations and Drug Claims

On June 24, 2014, the FDA issued a warning letter to Albert Max Inc.

Recalls & Warnings

7/01/2014

Maker of Elderberry Concentrate Warned for Manufacturing Violations

On June 23, 2014, the FDA issued a warning letter to Wyldewood Cellars Inc.

Recalls & Warnings

12/05/2014

Maker of Immune Supplement Warned for Manufacturing Violations

On November 20, 2014, the FDA issued a warning letter to Urban Moonshine, Inc.

Recalls & Warnings

4/03/2014

Maker of Green Coffee Bean Extract and Weight Loss Supplement Warned for Manufacturing Violations

On March 13, 2014, the FDA issued a warning letter to Libi Labs, Inc.

Recalls & Warnings

3/21/2014

Homeopathic Products Recalled Due to Allergy Risk

On March 20, 2014, Terra-Medica, Inc. issued a voluntary recall of 56 lots of homeopathic products including, Pleo-FORT, Pleo-QUENT, Pleo-NOT, Pleo-STOLO, Pleo-NOTA-QUENT, and Pleo-EX.

Recalls & Warnings

3/19/2014

Maker of Herbal Capsules and Extracts Warned for Manufacturing Violations

On September 19, 2013, the FDA issued a warning letter to Herbalist and Alchemist, Inc.

Recalls & Warnings

12/05/2012

Hydroxycut Class Action Lawsuit To Be Settled

Iovate Health Sciences Inc. has agreed to a settlement of $25.3 million, pending final court approval, in a class action lawsuit that alleged the company deceived consumers about the safety of its Hydroxycut weight loss supplements.

Recalls & Warnings

11/28/2012

Maker of Pycnogenol, Memory and Immune Supplements Warned For Manufacturing Violations and Misbranding

On November 15, 2012, the FDA issued a warning letter to contract manufacturer Health Technology, Inc.

Recalls & Warnings

1/16/2013

Nutrition Bars Recalled Due To Undeclared Allergen

On January 15, 2012, Belmont Confections Inc. issued a voluntary recall of Dymatize Nutrition Elite Gourmet Cookies & Cream bars and Dymatize Nutrition Elite Gourmet Fudge Brownie bars because they may contain undeclared peanuts.

Recalls & Warnings

11/14/2012

Mushroom Supplement Manufacturer Warned For Drug Claims and Adulteration

On October 18, 2012, the FDA issued a warning letter to Mushroom Wisdom, Inc. following a facility inspection and product label review which found the dietary supplements Amyloban 3399 From Lion's Mane, Grifron Maitake, and Super Shiitake to be promoted as drugs.

Recalls & Warnings

2/04/2013

Protein Supplement Recalled Due To Undeclared Soy and Milk

On January 30, 2013, R-Kane Products, Inc. issued a recall of Z PRO HIGH PROTEIN SUPPLEMENT after an FDA inspection found the potential allergens soy and milk were not listed on individual packet labels of the supplement.

Recalls & Warnings

5/03/2013

Maker of Probiotic, Iron and Folic Acid Supplements Warned For Manufacturing Violations

On April 17, 2013, the FDA issued a warning letter to Hillestad Pharmaceuticals USA, Inc.

Recalls & Warnings

2/28/2013

Maker of Liquid Omega-3 Supplements Warned For Manufacturing Violations

On February 20, 2013, the FDA issued a warning letter to Capco Custom Packaging Inc.

Recalls & Warnings

2/15/2013

Energy Drink Recalled Due To Bacterial Contamination

On December 21, 2012, NBTY issued a voluntary recall of the energy supplement MET-Rx Extreme Thermo Rage Watermelon 8 fl. oz. (Manufactured by MET-Rx Nutrition, Inc.) due to bacterial contamination.

Recalls & Warnings

2/14/2013

Protein Drink Recalled Due To Bacterial Contamination

On December 21, 2012, NBTY issued a voluntary recall of PURE PROTEIN PROTEIN SHOT 25g PROTEIN, GRAPE Flavor PROTEIN DRINK 2.9 fl. Oz. (Manufactured by Worldwide Sport Nutritional Supplements, Inc.) due to potential bacterial contamination.

Recalls & Warnings

4/19/2013

Recall: Contaminated Iron Supplement

On March 18, 2013, Magno Humphries Inc. issued a voluntary recall of Ferrous Sulfate Tablets 325 mg (5 Grain) , an iron dietary supplement, after the company discovered it was contaminated with small blue pieces of polypropylene, a kind of plastic.

Recalls & Warnings

6/12/2013

Biotin Supplement Found To Contain Only 4% to 5% of Labeled Amount

On May 22, 2013, the FDA issued a warning letter to Metaugus, Inc., following a facility inspection which found the company’s BIOTIN 3,000 mcg to be misbranded. The product's label was found to be false and misleading, and did not provide information required by federal regulations.

Recalls & Warnings

10/25/2013

Supplement Company Warned For Numerous Manufacturing Violations

On August 2, 2013, the FDA issued a warning letter to DNE Nutraceuticals, Inc., following a facility inspection which found the company's products to be adulterated because they were packed, or held under conditions that violate Current Good Manufacturing Practices for dietary supplements.

Recalls & Warnings

8/28/2013

Maker of Sexual Enhancement Supplement Warned for Manufacturing Violations

On July 11, 2013, the FDA issued a warning letter to Precise Nutrition International Inc.

Recalls & Warnings

3/04/2003

U.S. Marshalls Seize Supplements Claiming to Prevent Cancer and Treat Arthritis

On February 12, 2003, at the request of the Food and Drug Administration (FDA), U.S. Marshals seized dietary supplement products from Global Source Management and Consulting, Inc., in Sunrise, Florida. U.S.

Recalls & Warnings

6/30/2002

Recall of Dalyvite Liquid Multivitamin

In its June 26, 2002 Enforcement Report, the U.S. FDA reported the following Class III Food Recall. A Class III recall is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.

Recalls & Warnings

5/15/2016

Sexual Enhancement Supplements Recalled

On May 10, 2016, SOS Telecom, Inc. issued a recall of the following sexual enhancement supplements, which were found to contain undeclared sildenafil:

Recalls & Warnings

5/10/2016

Multis and Energy Mixes Recalled

On May 9, 2016, Let's Talk Health, Inc. issued a recall of the following supplements because they contain the undeclared allergens soy and milk: 

Recalls & Warnings

4/16/2016

Workout Supplement Containing Acacia Rigidula Recalled

On March 18, 2016, Nubreed Nutrition, Inc. issued a recall of all lots of its "pre-workout" supplement Undisputed which is labeled as containing Acacia rigidula, an ingredient which is not permitted in dietary supplements. 

Recalls & Warnings

4/06/2016

FDA Warns of Stimulant Methylsynephrine In Supplements

On March 31, 2016, the FDA issued warning letters to seven companies selling products containing methylsynephrine (also called p-hydroxyephedrine or Oxilofrine), a stimulant drug which is not permitted in dietary supplements in the U.S.

Recalls & Warnings

3/29/2016

Maker of Bone Health, Prostate, Cholesterol Supplements and More Warned for Drug Claims

On March 17, 2016, the FDA issued a warning letter to Rx Vitamins, Inc., following a facility inspection which found the company's products, includingTestost-Rx, DB-7, The Bone Density Formula, NaturLo Cholesterol, ThyRx-7 and Arth-9 to be misbranded.

Recalls & Warnings

3/15/2016

FDA Warns Sellers of Weight and Workout Supplements Containing Acacia Rigidula

On March 7, 2016, the FDA issued warning letters to five sellers of supplements which were labeled as containing Acacia rigidula, an ingredient which is not permitted in dietary supplements.

Recalls & Warnings

5/24/2016

Seller of Joint Health, Omega-3 Supplements & More Warned for Manufacturing Violations, Drug Claims

On May 13, 2016, the FDA issued a warning letter to Rocky Fork Formulas, Inc.

Recalls & Warnings

2/23/2016

Flax Seed and Chia Powders Recalled

On February 20, 2016, HEALTH MATTERS AMERICA INC., issued a recall of specific lots of Organic Traditions Sprouted Flax Seed Powder and Organic Traditions Sprouted Chia & Flax Seed Powder because they have the potential to be contaminated with Salmonella.

Recalls & Warnings

2/06/2016

Seller of Turmeric, Milk Thistle and More Warned for Manufacturing Violations, Drug Claims

On January 15, 2016, the FDA issued a warning letter to Terra Firma Botanicals, Inc.

Recalls & Warnings

10/18/2016

Seller of Sublingual Vitamins Warned for Drug Claims

On August 31, 2016, the FDA issued a warning letter to Bio-Stasis International, Inc., following a review of the company's website which found statements made about its sublingual tablets, ViraPress, Vitamin D-3 and Vitamin B-12. to be drug claims.

Recalls & Warnings

10/08/2016

Seller of Cell Power and Super Silica Warned for Manufacturing Violations, Misbranding

On September 23, 2016, the FDA issued a warning letter to SSO, Inc.

Recalls & Warnings

10/04/2016

Turmeric Spice Recalled Due to Elevated Lead Levels

On September 26, 2016, Spices USA Inc. issued a recall of 772 bags of TASTY SAWA GROUND TURMERIC because it contains elevated levels of lead.

Recalls & Warnings

9/14/2016

Seller of Aloe, Prostate and Joint Supplements Warned for Manufacturing Violations

On April 8, 2016, the FDA issued a warning letter to Salud Natural Entrepreneurs, Inc.

Recalls & Warnings

9/02/2016

Maker of Prescription Multi to Pay $15.5 Million to Settle Lawsuit Over Ingredient Claim

Endo Health Solutions Inc. has reportedly agreed to pay $15.5 million to settle a class action lawsuit which alleged its Qualitest Multi-Vitamin with Fluoride Chewable Tablets contained just 44% of the fluoride claimed on the label.

Recalls & Warnings

8/31/2016

Seller of Joint Supplement Warned for Manufacturing Violations, Drug Claims

On July 15, 2016, the FDA issued a warning letter to Vitalife Inc.

Recalls & Warnings

8/23/2016

Seller of Aloe Liquid and Capsules Warned for Manufacturing Violations, Drug Claims

On July 15, 2016, the FDA issued a warning letter to Aloe Farms, Inc.

Recalls & Warnings

8/08/2016

Turmeric Spice Recall Expanded to Include More Brands

On August 5, 2016, Gel Spice, Inc. expanded its recall of one lot of Fresh Finds Ground Turmeric Powder to include other turmeric spices sold under different brand names due to elevated levels of lead.

Recalls & Warnings

8/05/2016

More Turmeric Spice Recalled

On August 5, 2016, JM Exotic Foods, Inc. issued a recall of ground turmeric because it was found to contain elevated levels of lead.

Recalls & Warnings

7/29/2016

Ground Turmeric Spice Recalled Due to Lead Contamination

On July 28, 2016, Gel Spice, Inc. issued a voluntary recall one lot of Fresh Finds Ground Turmeric Powder because it was found to contain elevated levels of lead.

Recalls & Warnings

7/23/2016

Maker of "Super Food" Warned for Manufacturing Violations

On July 12, 2016, the FDA issued a warning letter to TerraVare, Inc.

Recalls & Warnings

7/16/2016

Herbalife Agrees to Business Restructure and $200 Million Payment to Settle FTC Charges of Deception

Herbalife and its associated companies (Herbalife International America Inc., Herbalife , Ltd.) has agreed to restructure its U.S.

Recalls & Warnings

1/21/2017

Seller of "Cancer Kits," Alpha Lipoic Acid Supplements and More Warned for Drug Claims

On December 22, 2016, the FDA issued a warning letter to Northern Health Products, Inc. following a review of the company's websites, www.northernhealthproducts.com and www.petdca.

Recalls & Warnings

12/03/2016

Male Enhancement Supplement Recalled

On November 29, 2016, MS Bionic, Inc. issued a recall of all lots of Megajex Natural Male Sex Enhancer capsules because they were found to contain tadalafil and sildenafil.

Recalls & Warnings

11/25/2016

DMAA Product Recalled

On November 23, 2016, NutriVitaShop (a dba of Naturecom Inc.) issued a recall of its DMAA net weight 500g because it may contain DMAA.

Recalls & Warnings

11/19/2016

GNC Women's Multi Recalled Due to Undeclared Allergen

On November 16, 2016, Nutra Manufacturing, Inc. issued a recall of one lot of GNC Women's Ultra Mega Time Release multivitamin because it contains undeclared milk.

Recalls & Warnings

8/31/2004

Two Makers of Weight Loss and Sex Enhancement Supplements Stopped From Making Unsubstantiated Claims

On August 27, 2004, the Federal Trade Commmission (FTC) reported that two Maine-based dietary supplement marketers and their principals have agreed to settle FTC charges that they made deceptive advertising claims about their dietary supplement products, in violation of federal law.

Recalls & Warnings

7/21/2003

FTC Stops False Advertising of Heavily Promoted Supplements for Breast Enhancment, Male Virility, and Snoring

On June 10, 2003, the Federal Trade Commission (FTC) announced that infomercial marketers Wellquest International, Inc. and Tony Hoffman Productions, Inc.

Recalls & Warnings

5/17/2002

Update on Recall of Certain Ultra Slim-Fast with Soy Protein Drinks

In its May 15, 2002 Enforcement Report, the U.S. FDA reported the following Class III Food Recall. A Class III recall is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.

Recalls & Warnings

5/03/2002

More Information on Recall of PC-SPES - Prostate Supplement

The FDA's May 1, 2002 Enforcement Report classified the recall of PC-SPES as a Class I recall. The recall was originally announced by its manufacturer in February with additional warnings from the FDA issued in March (see the 3/11/02 posting on ConsumerLab.

Recalls & Warnings

2/03/2016

Seller of Weight and Enhancement Supplements Warned For Drug Claims

On December 11, 2015, the FDA issued a warning letter to The One Minute Miracle, Inc., following a review of the company's website which found statements made about   Miracle Diet 30 and Miracle Rock 48 to be drug claims.

Recalls & Warnings

1/26/2016

Seller of CoQ10, SAM-e, Vitamin D, and More Warned for Manufacturing Violations, Drug Claims

On January 15, 2016, the FDA issued a warning letter to Nutri-Dyn Midwest, Inc., following a facility inspection which found the company's products, including Cardioauxin BP, Zinc Lozenge, Oliver, Pau D'Arco, Petadolex, Chondro Jointaide, Dynagesic, SAMe-200, Gugulipid.

Recalls & Warnings

1/21/2016

Morphine Found in Licorice Product

On January 20, 2016, Master Herbs, Inc. issued a recall of all lots of Licorice Coughing Liquid because it was found to contain morphine.

Recalls & Warnings

1/20/2016

Maker of Growth Hormone, Testosterone Booster Warned for Manufacturing Violations, Misbranding

On January 8, 2016, the FDA issued a warning letter to Nutraloid Labs Inc.

Recalls & Warnings

1/16/2016

Seller of Liver, Lung Support Supplements Warned for Drug Claims

On January 4, 2016, the FDA issued a warning letter to Tibetan Herbal Balance, Inc.

Recalls & Warnings

12/29/2015

Maker of Vitamin K, Vitamin A & More Warned for Manufacturing Violations, Drug Claims

On December 10 2015, the FDA issued a warning letter to Dherbs Health Emporium, Inc.

Recalls & Warnings

12/12/2015

Sexual Enhancement Supplement Recalled

On December 11, 2015, Reesna Inc. issued a recall of its sexual enhancement supplements Fuel Up Plus and Fuel Up High Octane which were distributed in August 2015 and were found to contain undeclared hydroxythiohomosildenafil.

Recalls & Warnings

9/07/2002

FDA Sends Warning Letters to Seven Online Supplement Sellers For Therapeutic Claims

On August 27, 2002, the FDA posted seven "Cyber" letters recently issued from its Center for Food Safety and Applied Nutrition (CFSAN) to internet website operators promoting dietary supplement products that claim to diagnose, mitigate, treat, cure, or prevent a specific disease or class of ...

Recalls & Warnings

10/10/2003

Government Stops Sale of Supplements Claiming to Treat Obesity and Impotence

On October 8, 2003, The Food and Drug Administration (FDA) announced that on September 22, 2003, U.S. District Court Judge Robert J. Vining, Jr.

Recalls & Warnings

6/23/2003

FDA Warns Consumers Against Taking 6 Sexual Enhancement Supplements

On June 20, 2003, the Food and Drug Administration (FDA) warned consumers not to purchase or consume the following products: SIGRA, STAMINA Rx and STAMINA Rx for Women, Y-Y, Spontane ES and Uroprin, manufactured by NVE, Inc., in Newton, N.J. and distributed by Hi-Tech in Norcross, Ga.

Recalls & Warnings

7/15/2004

Company Stopped by FTC from Claiming to Prevent or Reverse Memory Loss without Evidence

On July 13, 2004, the Federal Trade Commission(FTC) announced that a dietary supplement manufacturer has settled FTC charges that it violated federal law by making unsubstantiated claims that its product, “Senior Moment,” could prevent memory loss and restore memory function in adults.

Recalls & Warnings

6/21/2005

Marketers of “Himalayan Diet Breakthrough” Settle FTC Charges of Deceptive Advertising

On June 20, the Federal Trade Commission (FTC) announced that AVS Marketing, Inc., and its president, William R. Heid, have agreed to pay $400,000 in consumer redress to settle FTC charges that they deceptively marketed a purported weight-loss pill called “Himalayan Diet Breakthrough.

Recalls & Warnings

8/28/2008

FDA Finds Fault with Generic Toprol XL -- Problems Reported Earlier by ConsumerLab.com

On August 12, 2008, the U.S. FDA sent a letter to Sandoz Inc. warning of violations in its manufacture of Metoprolol Succinate ER tablets and other drug products. Sandoz's Metoprolol Succinate ER tablets are generic versions of Toprol XL.

Recalls & Warnings

3/19/2009

QVC Settles Charges of False Claims for Supplements

On March 19, 2009, the Federal Trade Commission (FTC) announced that QVC, Inc., a TV home shopping channel and one of the world’s largest multimedia retailers, has agreed to pay $7.

Recalls & Warnings

5/17/2007

Recall of Shark Cartilage Due to Potential Contamination

On May 16, 2007, NBTY, Inc.

Recalls & Warnings

11/28/2006

FTC Targets Seller of Pills Promoted for Height, Weight, and Bone Improvement

On November 28, 2006, the Federal Trade Commission (FTC) announced that a Florida business and its owner, who marketed purported height-enhancing pills for kids and young adults, will pay $375,000 to settle charges that their advertising claims were deceptive.

Recalls & Warnings

3/08/2007

FTC Files Against Maker of Calcium and Fertility Supplements

On January 29, 2007, the Federal Trade Commission (FTC) announced that it had filed civil contempt charges against Lane Labs, Inc.

Recalls & Warnings

9/16/2005

FTC Stops Weight-loss Claims about Seaweed-based Patches

On September 15, 2005, the U.S. Federal Trade Commission (FTC) announced that the alleged masterminds behind a fraudulent scheme to market two seaweed-based patches as weight-loss products to U.S. consumers have settled FTC charges.

Recalls & Warnings

10/15/2007

US Marshalls Seize Charantea Supplements Promoted for Diabetes, Anemia and Hypertension

At the request of the U.S. Food and Drug Administration (FDA), on October 9, 2007, U.S. Marshals seized approximately $71,000 of goods from FulLife Natural Options, Inc., of Boca Raton, Fla., which marketed and distributed Charantea Ampalaya Capsules and Charantea Ampalaya Tea.

Recalls & Warnings

7/19/2011

FDA Warns of Unsafe Drug in Slimming Supplements

On July 8, 2011, the U.S. FDA advised consumers not to purchase or use Slim Forte Slimming Capsule and Slim Forte Double Power Slimming Capsules. FDA laboratory analysis confirmed that these products contain sibutramine. Sibutramine is a controlled substance that was removed from the U.S.

Recalls & Warnings

10/05/2011

FDA Warns Herbal Nitro of Manufacturing Violations

The FDA has published a Warning Letter dated September 22, 2011 to Herbal Nitro Inc. regarding manufacturing violations at its facility in Yucaipa, CA.

Recalls & Warnings

3/28/2011

FDA Cracks Down on Violators of Supplement Manufacturing Rules

In February and March 2011, the U.S. FDA posted Warning Letters sent, respectively, to a distributor of dietary supplements and a supplement manufacturer for violations of current Good Manufacturing (GMP) rules.

Recalls & Warnings

2/24/2011

Recall of Counterfeit Extenze Tablets Containing Drugs

On February 23, 2011, the FDA announced that Biotab Nutraceuticals, Inc. was notified that two lots of counterfeit product purporting to be Extenze contain undeclared drug ingredients. Specifically, lot 0709241 contains tadalafil and sildenafil, and lot 0509075 contains tadalafil and sibutramine.

Recalls & Warnings

6/21/2011

FDA Warns Laboratory of Manufacturing Violations

On June 10, 2011, the U.S. FDA posted a Warning Letter (dated 4/15/11) to Nutro Laboratories, a division of NBTY, Inc., concerning serious violations of the current Good Manufacturing Practice (CGMP) regulations for Dietary Supplements based on its inspection of Nutro facilities in October 2010.

Recalls & Warnings

6/07/2011

FDA Seizes Elderberry Juice Concentrate Due to Unproven Claims

On June 3, 2011, The U.S. FDA announced that, at its request, U.S. Marshals seized elderberry juice products that have been distributed by Wyldewood Cellars Inc., based in Peck, Kan., because the products are unapproved and misbranded drugs.

Recalls & Warnings

6/01/2011

FDA Finds Pesticides in Ginseng Supplement

The U.S. FDA found pesticides in Root to Health, American Ginseng, Herbal Supplement (500 Veggie Capsules, 500 mg each) according to a May 13, 2011 Warning Letter from the FDA to the manufacturer of the product, Hsu's Ginseng Enterprises, Inc.

Recalls & Warnings

6/24/2010

FDA Warns Seller of Pills Used to Treat Autism

On June 17, 2010 the U.S. Food and Drug Administration (FDA) sent a Warning Letter of legal violations to CTI Science, Inc., the marketer of OSR#1. The product is marketed as a supplement, but contains an ingredient that is not legally permitted to be sold as a supplement.

Recalls & Warnings

5/03/2010

FDA Warns Consumers to Avoid Breath Supplement Contaminated with Lead

On May 3, 2010 the U.S. Food and Drug Administration warned consumers not to purchase nor consume Vita Breath, a dietary supplement manufactured by American Herbal Lab Inc. of Rosemead, Calif.

Recalls & Warnings

4/07/2010

Nationwide Recall of Masxtreme Capsules Containing Drugs with Cardiovascular Side Effects

On March 30, 2010, the U.S. Food and Drug Administration (FDA) posted a notice from Natural Wellness warning consumers not to purchase or consume the product known as MasXtreme, Lot# 911035.

Recalls & Warnings

2/17/2010

FTC Warns of Deceptive Claims with Children's Omega-3 Supplements

On February 17, 2010, the Federal Trade Commission (FTC) announced that it had sent letters to 11 companies that promote various omega-3 fatty acid supplements, telling them they should review their product packaging and labeling to make sure they do not violate federal law by making baseless ...

Recalls & Warnings

9/13/2010

ExtenZe Enhancement Supplements Seized in Canada

On August 19, 2010, Health Canada (Canada's health ministry) seized the sexual enhancement supplements "Male Enhancement ExtenZe" and "Women ExtenZe" which were imported from the U.S. Although legal and widely sold in the U.S.

Recalls & Warnings

10/08/2010

FDA Warns of Stimulant in Slimming Capsules

On October 8, 2010, the U.S. FDA advised consumers who have Slimming Beauty Bitter Orange Slimming Capsules not to use the product. FDA warns that Slimming Beauty Bitter Orange Slimming Capsules contain the active pharmaceutical ingredient sibutramine, a prescription-only drug which is a stimulant.

Recalls & Warnings

12/14/2009

Nationwide Recall of Sexual Enhancement Supplements Containing Drug-like Compound

On December 14, 2009, the Federal Drug Administration (FDA) posted a notice on its website regarding the recall of many sexual enhancement supplements sold by Atlas Operations, Inc.

Recalls & Warnings

9/07/2012

Prebiotics Recalled For Salmonella Risk

On September 4, 2012, Eco Health, Inc. announced a recall of its florAlign Prebiotic Formula (Powder) due to the potential for the product to be contaminated with Salmonella.

Recalls & Warnings

9/21/2012

Sexual Enhancement Supplements For Men and Women Recalled Due to Prescription Drug Risk

On August 23, 2012, Evol Nutrition Associates Inc./Red Dawn issued a voluntary recall of Mojo Nights after FDA testing revealed the male sexual enhancement supplement contains undeclared prescription drugs tadalafil and sildenafil.

Recalls & Warnings

9/18/2012

Men’s Sexual Enhancement Supplement Containing Prescription Drug Recalled

On September 12, 2012, Body Basics Inc. issued a voluntary nationwide recall of ACTRA-Sx 500 Dietary Supplement Capsules after independent laboratory testing confirmed the supplement contains the prescription drug sildenafil citrate.

Recalls & Warnings

9/18/2012

Maker of Noni, Nopal, Blood Sugar and Cholesterol Supplements Warned For Drug Claims, Misbranding, and Manufacturing Violations

On August 27, 2012, the FDA issued a warning letter to Naturavit, Inc. for making statements about dietary supplements Noni Imperial Hawaiian, Garlic and Parsley, Cholestol, Nopal and Diatrin that constitute drug claims.

Recalls & Warnings

8/29/2012

Herbal Supplement Company Warned For Medical Claims

On August 2, 2012, the FDA issued a warning to HSAC Enterprises, Inc. dba Kare-N-Herbs subsequent to a facility inspection and website review in May 2012 which found statements made about Kold Kare, Energy Kare and Tranquility Kare dietary supplements to constitute drug claims.

Recalls & Warnings

10/24/2012

Warning Issued to Memory Supplement Maker For Unapproved Drug Ingredient, Drug Claims and Unreported Adverse Events

On October 16, 2012, the FDA issued a letter to dietary supplement manufacturer Quincy Bioscience Manufacturing Inc.

Recalls & Warnings

10/18/2012

Natural Product Manufacturer Warned For GMP Violations, Misbranding, Unapproved Devices and Drug Claims

On August 28, 2012, the FDA issued a warning letter to Creation's Garden Natural Products, Inc. following an inspection of the company's manufacturing facility, which found violations of Current Good Manufacturing Practices (CGMPs) for dietary supplements.

Recalls & Warnings

8/09/2012

Makers of Mineral Water Containing Lithium Warned

On July 20, 2012, the FDA issued a warning letter to Lithia Mineral Water, Inc. declaring Lithia mineral water product to be an approved drug following a 2011 facility inspection.

Recalls & Warnings

3/03/2012

Seller of Cancer Cures Warned by FDA

On February 9, 2012, the U.S. FDA sent a Warning Letter to BioAnue Laboratories, Inc. informing it that its websites at www.tumorx.com, www.cancerx.org, www.hopewelltechnologieslimited.com, and www.vmhe.

Recalls & Warnings

3/09/2012

Maker of Inhaled Caffeine Product Gets Warning

The U.S. FDA issued a Warning Letter to Breathable Foods, Inc. (dated March 5, 2012) advising that their product AeroShot, which is promoted for "breathable energy," is falsely labeled (misbranded).

Recalls & Warnings

4/16/2012

Protein Supplement Maker Fails FDA Audit -- Many Products Affected

The FDA sent a Warning Letter (dated April 2, 2012) to Theta Brothers Sports Nutrition, Inc. regarding numerous violations of good manufacturing practices at its Lakewood, New Jersey facility.

Recalls & Warnings

3/02/2012

Recall of Enhancement Supplement for Men -- Contains Drug

On Feb, 24, 2012, Regeneca, Inc. announced a voluntary nationwide recall of all lots of RegenErect. The product was distributed throughout the U.S. and Puerto Rico to Internet consumers. The product is distributed as a blue capsule sold individually in foil packets with a UPC code of 816860010055.

Recalls & Warnings

2/17/2012

FDA Warns Supplement Company of Manufacturing Violations

The U.S. FDA recently posted a Warning Letter to Pure Encapsulations, Inc.

Recalls & Warnings

2/16/2012

Recall of Enhancement Supplement for Women -- Contains Drug

On Feb, 10, 2012, Regeneca, Inc. announced a voluntary nationwide recall of RegenArouse Natural Female Intimacy Enhancement. The product was distributed throughout the U.S. and Puerto Rico to Internet consumers. The product is distributed as a pink capsule sold individually in foil packets.

Recalls & Warnings

2/11/2012

Herbal Sprays for Colds and Cold Sores Recalled

On February 10, 2012 the U.S. FDA posted a notice announcing the recall of all "Koff & Kold" and "Kold Sore" sprays by Wholistic Herbs Inc. The products were distributed throughout the United States.

Recalls & Warnings

1/17/2012

Recall of Calcium-Vitamin D Product That's Actually Glucosamine -- Allergy Alert

As published on the U.S. FDA's website, Rexall Inc. announced a recall on January 16, 2012 of Rexall Calcium 1200 mg plus 1000 IU Vitamin D3, 60 softgels. The affected bottles actually contain a TABLET product, Triple Strength Glucosamine Chondroitin and MSM Tablets.

Recalls & Warnings

8/27/2013

FTC Refunds Consumers of Children's Vitamins as Part of Deceptive Advertising Settlement

On August 8, 2013, the Federal Trade Commission (FTC) announced it has mailed 10,144 refund checks to consumers who purchased Disney or Marvel Hero -themed children's vitamins, including Disney Princesses, Winnie the Pooh, Finding Nemo, and Spider-Man varieties, between May 1, 2008 and September ...

Recalls & Warnings

8/23/2013

Sexual Enhancement Supplement Containing Undeclared Drugs Recalled

On August 12, 2013, Jack Rabbit Inc. issued a voluntary recall of one lot of sexual enhancement supplement Jack Rabbit because it was found to contain undeclared sildenafil and tadalafil.

Recalls & Warnings

8/16/2013

Maker of Energy, Weight Loss, Sleep and Vitamin D Supplements Warned for Manufacturing Violations

On July 22, 2013, the FDA issued a warning letter to N.V.E. Pharmaceuticals, Inc.

Recalls & Warnings

8/29/2013

Seller of CELLFOOD Supplements Warned For Manufacturing Violations and Drug Claims

On August 1, 2013, the FDA issued a warning letter to supplement retailer Lumina Health Products, Inc.

Recalls & Warnings

1/04/2014

Smoking Cessation and Anti-Inflammatory Supplements Contain Unapproved Ingredient

On December 13, 2013, the FDA issued a warning letter to Star Scientific, Inc. after the agency noted that the company's smoking cessation supplement CigRx and anti-inflammatory supplement Anatabloc contain anatabine, a chemical not currently allowed in dietary supplements.

Recalls & Warnings

12/26/2013

Weight Loss Supplement Recalled

On December 23, 2013, Deseo Rebajar Inc. issued a voluntary recall of one lot of Burn 7 Capsules because they were found to contain sibutramine.

Recalls & Warnings

12/19/2013

Seller of Sexual Enhancement Supplement and Tea Drink Warned for Drug Ingredients and Drug Claims

On December 5, 2013, the FDA issued a warning letter to Green Planet, Inc. following a facility inspection which found the company's sexual enhancement supplement Night Bullet to contain the drugs sulfohydroxyhomosildenafil, thioaildenafil and aminotadalafil.

Recalls & Warnings

12/16/2013

Weight Loss Capsules Recalled Due Allergen Risk

On December 13, 2013, Stone Independent Research, Inc. issued recall of one lot of Zanocap Scientific Weight Loss 500 mg capsules because they contain undeclared whey protein, which is derived from milk.

Recalls & Warnings

12/13/2013

Maker of Menopause Blend and Other Supplement Ingredients Warned by FDA of Violations

On November 21, 2013, the FDA issued a warning letter to Raw Deal, Inc.

Recalls & Warnings

11/21/2013

Weight Loss Supplement Recalled

On November 14, 2013, Deseo Rebajar Inc. issued a recall of one lot of weight loss supplement Adipotrim XT because it was found to contain undeclared fluoxetine.

Recalls & Warnings

11/20/2013

$2 Million In Weight Loss and "Fat-Burning" Supplements Seized

On November 12, 2013, U.S. Marshals seized more than $2 million worth of supplements from Georgia-based Hi-Tech Pharmaceuticals, Inc.

Recalls & Warnings

10/12/2013

Metagenics Enzyme Supplement Recalled Due To Drug Risk

On October 11, 2013, Metagenics Canada issued a voluntary recall of digestive enzyme supplement Spectrazyme, due to potential contamination with the prescription antibiotic chloramphenicol.

Recalls & Warnings

10/11/2013

Prebiotic and Digestive Enzyme Supplement Recalled Due To Drug Risk

On October 10, 2013, Adeeva Nutritionals Inc. issued a voluntary recall of digestive supplement Flora Essentials due to potential contamination with the prescription antibiotic chloramphenicol.

Recalls & Warnings

9/27/2013

Company Warned For Distributing Weight Loss Supplement Containing DMAA, Drug Claims

On September 6, 2013, the FDA issued a warning letter to Pure Energy Products, Inc., following a facility inspection which found that the company distributes a weight loss supplement, called obestrim, which contains dimethylamylamine, or DMAA.

Recalls & Warnings

6/12/2013

Weight Loss Supplement Recalled Due To Undeclared Drugs

On June 11, 2013, Bethel Nutritional Consulting, Inc. issued a voluntary recall of one lot of Bethel 30 herbal weight loss supplement because it was found to contain undeclared sibutramine and phenolphthalein.

Recalls & Warnings

6/07/2013

Maker of Colloidal Silver and Mushroom Extract Supplements Warned For Manufacturing Violations and Drug Claims

On May 2, 2013, the FDA issued a warning letter to Earthborn Products, Inc.

Recalls & Warnings

5/29/2013

Seller of Colloidal Silver, Noni Juice and Noni Supplements Warned For Drug Claims

On May 16, 2013, the FDA issued a warning letter to Matrix Health Products, Inc.

Recalls & Warnings

5/24/2013

Seller of Liquid Minerals, Joint Care and Herbal Supplements Warned For Manufacturing Violations, Drug Claims

On April 8, 2013, the FDA issued a warning letter to Body Systems, Inc.

Recalls & Warnings

5/23/2013

Maker of Liver Detox and Insulin Supplements Warned For Drug Claims

On April 24, 2013, the FDA issued a warning letter to Glucorell, Inc.

Recalls & Warnings

5/17/2013

Maker of Cardio, Arthritis, Cleanse Supplements and More Warned For Manufacturing Violations and Drug Claims

On May 8, 2013, the FDA issued a warning letter to Entrenet Nutritionals, Inc.

Recalls & Warnings

5/17/2013

Hoodia, Sexual Enhancement Supplements and More Found To Be Adulterated, Misbranded

On March 01, 2013, the FDA issued a warning letter to Desert Rose Manufacturing, Inc.

Recalls & Warnings

4/18/2013

Cardio, Energy and Sexual Enhancement Supplement Distributor Warned For Manufacturing Violations and Drug Claims

On December 21, 2012, the FDA issued a warning letter to ForMor Inc, dba ForMor International, following a facility inspection which found the company's Cardio Cocktail and Argenix dietary supplements to be adulterated because because they were prepared, packed, or held under conditions that do ...

Recalls & Warnings

4/11/2013

Maker of Workout Booster Warned For Manufacturing Violations

On March 5, 2013, the FDA issued a warning letter to Primarch Manufacturing, Inc.

Recalls & Warnings

4/10/2013

Recall: Sexual Enhancement Supplement Containing Undeclared Drug

On April 1, 2013, Consumer Concepts, Inc. issued a voluntary nationwide recall of ROCK-It MAN Male Enhancement Capsules, a dietary supplement promoted for sexual enhancement which was found to contain undeclared hydroxythiohomosildenafil, an analogue of the prescription drug sildenafil.

Recalls & Warnings

7/12/2013

Herbal Supplement Company Warned For Drug Claims, Manufacturing Violations

On June 18, 2013, the FDA issued a warning letter to Herbs of Light, Inc.

Recalls & Warnings

7/05/2013

Seller of Vision Supplement Warned For Drug Claims

On June 25, 2013, the FDA issued a warning letter to Nutrient Synergy, Inc., following a review of the company's website which found statements made about the dietary supplement Nepretin to be drug claims.

Recalls & Warnings

8/06/2013

Weight Loss Supplement Recall Expanded

On August 5, 2013, Bethel Nutritional Consulting, Inc., issued a voluntary recall of herbal weight loss supplements Quick Thin and Bethel Advance because they were found to contain sibutramine and phenolphthalein.

Recalls & Warnings

2/14/2013

Maker of Antioxidant and Anti-Aging Supplements Warned For Manufacturing Violations

On January 10, 2013, the FDA issued a warning letter to dietary supplement manufacturer Consolidated Marketing Unlimited, Inc.

Recalls & Warnings

2/12/2013

Judge Orders Drug and Supplement Company to Cease Manufacturing and Distribution

On February 8, 2012, the FDA announced Titan Medical Enterprises Inc. has been ordered to stop manufacturing and distributing drugs and dietary supplements until the company's manufacturing operations comply with the Federal Food, Drug, and Cosmetic Act. The order was signed on December 11, 2012, U.

Recalls & Warnings

5/03/2013

Homeopathic Company Warned For Drug Claims and Improper Labeling

On March 12, 2013, the FDA issued a warning letter to Natural Medicine Associates, Inc.

Recalls & Warnings

2/28/2013

Maker of Joint, Mood and B Vitamin Supplements Warned For Manufacturing Violations, Misbranding and Drug Claims

On February 11, 2013, the FDA issued a warning letter to Kreativ Health, Inc.

Recalls & Warnings

3/22/2013

Maker of Nutrition Shakes Warned For Manufacturing Violations

On February 28, 2013, the FDA issued a warning letter to Healthwest Minerals, Inc., dba Mt. Capra Products, Mt. Capra Whole Foods, and Mt.

Recalls & Warnings

3/21/2013

Probiotic Recalled Due To Undeclared Soy

On March 20, 2013, New Chapter, Inc. issued a voluntary recall of one lot of its Probiotic Elderberry dietary supplement because it may contain undeclared soy.

Recalls & Warnings

3/13/2013

Recall: Male Sexual Enhancement Supplement Containing Drugs

On March 12, 2013, Green Planet, Inc. issued a recall of one lot of the male sexual performance enhancer supplement Night Bullet because it was found to contain trace amounts of sulfohydroxyhomosildenafil and aminotadalafil, analogues of the prescription drug sildenafil.

Recalls & Warnings

3/11/2013

Nutrition Bar Recalled Due To Undeclared Allergen

On March 7, 2013, Lifestyle Evolution Inc. issued a recall of various NuGO nutrition bars because the bars may contain undeclared milk, a potential allergen.

Recalls & Warnings

3/06/2013

Protein Bar Recalled Due To Salmonella Risk

On March 4, 2013, Pro-Amino International Inc. issued a recall of Proti Diet High Protein Chocolate Dream Bar due potential Salmonella contamination.

Recalls & Warnings

1/30/2013

Seller of Omega-3 and Emu Oil Supplements Warned For Drug Claims, Misbranding

On November 19, 2012, the FDA issued a warning letter to Emu Products & Management, Inc. after a review of the company's website found statements that promoted the dietary supplements Multi-Omega Gel Caps, Recovery Gel Caps, ARP Gel Caps and the topical skin products Extreme Cryo Gel, F.A.C.E.

Recalls & Warnings

1/18/2013

Recall: Iron Supplement Containing Motion Sickness Drug

On January 18, 2012, Advance Pharmaceutical Inc. announced the recall of one lot of Rugby NATURAL IRON SUPPLEMENT Ferrous Sulfate Tablets 325 mg, because the bottles were found to contain meclizine HCl 25 mg tablets instead.

Recalls & Warnings

12/19/2012

Sexual Enhancement Supplements Recalled Due To Undeclared Drugs

On December 17, 2012, Performance Plus Marketing, Inc.

Recalls & Warnings

11/21/2012

Maker of Blood Pressure, Probiotic, Resveratrol and Hormonal Supplements Warned For Manufacturing Violations and Drug Claims

On November 2, 2012, the FDA issued a warning letter to Atrium, Inc. following a facility inspection which found a number of the company's dietary supplements to be adulterated or promoted as drugs.

Recalls & Warnings

2/19/2014

Seller of Sexual Enhancement Supplements Warned For Manufacturing Violations

On February 11, 2014, the FDA issued a warning letter to Maximus Niterider International Group, Inc.

Recalls & Warnings

2/13/2014

Maker of Cholesterol and Workout Supplements Warned For Manufacturing Violations, Drug Claims and Unapproved Ingredient

On January 31, 2014, the FDA issued a warning letter to Exclusive Supplements Inc.

Recalls & Warnings

1/16/2014

Seller of Tea Supplements and Drinks Warned For Manufacturing Violations and Drug Claims

On December 31, 2013, the FDA issued a warning to Prestige Chinese Teas Company, Inc.

Recalls & Warnings

3/31/2014

Seven Sexual Enhancement Supplements Recalled Due to Undeclared Drugs

On March 27, 2014, Nova Products, Inc. issued a voluntary recall of sexual enhancement supplements African Black Ant, Black Ant, XZen Gold, ZXen Platinum, XZen 1200, XZone Gold and XZone 1200.

Recalls & Warnings

4/09/2014

Maker of Relaxation Drink Warned For Melatonin Ingredient

On March 27, 2014, the FDA issued a warning letter to Dewmar International BMC, Inc. following a review of the company's product packaging and labels, which found the "relaxation beverage" Lean Slow Motion ...

Recalls & Warnings

5/07/2014

Three Sexual Enhancement Supplements Recalled

On May 5, 2014 , Eugene Oregon, Inc. issued a precautionary, voluntary recall of sexual enhancement supplements African Black Ant, Black Ant and Mojo Risen.

Recalls & Warnings

5/01/2014

Weight Loss Supplement Recalled

On April 29, 2014, dietary supplement distributor Bacai Inc. issued a voluntary recall of one lot of weight loss supplement LiteFit USA because it was found to contain sibutramine.

Recalls & Warnings

4/29/2014

Seller of B Vitamins, CoQ10, Amino Acids and Other Supplements Warned for Manufacturing Violations and Drug Claims

On April 1, 2014, the FDA issued a warning letter to Bio-Recovery, Inc.

Recalls & Warnings

4/24/2014

Arthritis Supplement Containing Multiple Drugs Recalled

On April 21, 2014, Nano Well-being Health Inc., issued a voluntary recall of two lots of arthritis supplement Super Arthgold, because it was found to contain the drugs chlorzoxazone, diclofenac and indomethacin.

Recalls & Warnings

4/18/2014

FDA Questions Ingredient in Workout Supplement

On April 4, 2014, the FDA issued a warning letter to Driven Sports Inc., following a label review which found the company's workout supplement, CRAZE, to be adulterated because it contains the new dietary ingredient Dendrobex.

Recalls & Warnings

6/12/2014

Marketers of Memory Supplement Settle FTC Charges of Deceptive Claims

Martek Biosciences Corporation and i-Health Inc., marketers of BrainStrong Adult, have agreed to settle Federal Trade Commission (FTC) charges that claims the supplement could improve adult memory and prevent cognitive decline were deceptive, and not supported by sufficient clinical evidence.

Recalls & Warnings

6/05/2014

More Chia Powders Recalled Due to Salmonella Risk

On June 4, 2014, Health Matters America Inc. issued a voluntary recall its Organic Traditions Sprouted Chia Seed Powder and Organic Traditions Sprouted Chia & Flax Seed Powder because they have the potential to be contaminated with Salmonella.

Recalls & Warnings

5/31/2014

Sellers of "Cancer" Supplements Warned for Drug Claims

Two sellers of graviola supplements promoted to treat cancer have been issued warning letters by the FDA. Graviola (Annona muricata), also known as soursop, is the fruit of a tree native to South America and Puerto Rico.

Recalls & Warnings

5/30/2014

Seller of Brain, Diabetes, Echinacea Supplements and More Warned for Drug Claims

On April 22, 2014, the FDA issued a warning letter to Mundo Natural Inc., following a review of the company's website which found statements made about supplements Neuro AD, Stop Diabetes, Stop High Blood Pressure, Morninga 7 and Purpurea Echinacea to be drug claims.

Recalls & Warnings

5/29/2014

Recall of Sexual Enhancement Supplements Expanded

On May 28, 2014, Eugene Oregon, Inc. expanded its previous recall of certain lots of sexual enhancement supplements African Black Ant, Black Ant, and Mojo Risen. All lots of these supplements are now recalled.

Recalls & Warnings

5/21/2014

Seller of Gingko and Milk Thistle Warned for Manufacturing Violations and Drug Claims

On April 4, 2014, the FDA issued a warning letter to Xtra Life Natural Systems, Inc.

Recalls & Warnings

7/11/2014

Maker of Cough and Sleep "Remedies" Warned for Drug Claims

On June 27, 2014, the FDA issued a warning letter to Zarbee's, Inc.

Recalls & Warnings

11/17/2014

Probiotic Powder Recalled

On November 14, 2014, Solgar, Inc. issued a voluntary recall of Solgar ABC Dophilus Powder (NET Wt. 1.75 oz (50 g)) because it was found to contain Rhizopus oryzae, a fungus which may cause Mucormycosis infection.

Recalls & Warnings

11/11/2014

Maker of Children's Vitamins, Weight Loss Supplements and More Warned for Manufacturing Violations

On October 30, 2014, the FDA issued a warning letter to VitalHealth Tech, Inc., following a facility inspection which found the company's products, including Kids Mighty Vites tablets, Omni Jr.

Recalls & Warnings

12/07/2014

FDA Raises Concerns Over Generic ADHD Drugs

On November 13, 2014, the U.S.

Recalls & Warnings

10/21/2014

Seller of Weight Loss Supplements Warned for Manufacturing Violations and Drug Claims

On October 7, 2014, the FDA issued a warning letter to YoungYou International, Inc.

Recalls & Warnings

10/10/2014

Seller of Multivitamin Warned for Drug Claims

On September 25, 2014, the FDA issued a warning letter to Multimmunity, Inc., following a review of the company's website which found statements made about the dietary supplement Multimmunity to be drug claims.

Recalls & Warnings

9/30/2014

U.S. Marshals Seize $5 Million Worth of Kratom

On September 25, 2014, U.S. Marshals seized more than 25,000 pounds of raw kratom valued at over $5 million from Rosefield Management, Inc. in Van Nuys, California. The action was taken at the request of the FDA.

Recalls & Warnings

9/10/2014

Seller of Joint Pain Supplement Warned for Drug Claims

On August 24, 2014, the FDA issued a warning letter to CreAgri, Inc., following a website review, which found statements made about the company's products, including Olivenol plus Easeflex, Olivenol plus Essence Capsules, and Olivenol plus Essence Elixer, to be drug claims.

Recalls & Warnings

9/09/2014

Maker of Popular Green Coffee Bean Extract Settles FTC Charges of Unsupported Weight Loss Claims

Applied Food Sciences, Inc., maker of green coffee bean extract GCA, has agreed to pay $3.5 million to settle FTC charges that weight loss claims made about the extract were not supported by scientific evidence.

Recalls & Warnings

9/05/2014

Seller of "Nerve", "Cleanse" and Probiotic Supplements Warned for Drug Claims

On July 30, 2014, the FDA issued a warning letter to Plexus Worldwide, Inc., following a review of the company's website and product labels, which found statements made about Fast Relief, BioCleanse and ProBio5 to be drug claims.

Recalls & Warnings

8/21/2014

Seller of Joint Supplement Warned for Manufacturing Violations and Drug Claims

On July 17, 2014, the FDA issued a warning letter to Klein Laboratories, Inc.

Recalls & Warnings

7/30/2014

Chocolate and Carob Drink Mix Recalled Due To Salmonella Risk

On July 25, 2014, CaCoCo, Inc. issued a recall of CaCoCo Original and Global Warrior chocolate drink mixes because they contain organic carob powder which has the potential to be contaminated with Salmonella.

Recalls & Warnings

7/26/2014

Marketers of Nopal Cactus Drink Settle FTC Charges of Deceptive Claims

TriVita Inc., and marketers of the company's "prickly pear" fruit drink Nopalea have agreed to pay $3.5 million in consumer refunds to settle FTC charges they made deceptive claims that the drink treats health problems ranging from skin conditions to joint pain and respiratory problems.

Recalls & Warnings

7/26/2014

FTC Says Company Made "Outrageous" Weight Loss Claims

Marketers for the Canadian-based Freedom Center Against Obesity have agreed to pay $500,000 to settle FTC charges the company made deceptive claims about its Double Shot diet pills.

Recalls & Warnings

8/22/2015

Synthetic Amphetamine, Less Protein and More Sugar Than Claimed Found in Workout Supplements

On August 7, 2015, the FDA issued a warning letter to New Dawn Nutrition, Inc.

Recalls & Warnings

8/04/2015

Whey, Casein and Colostrum Products Recalled

On August 3, 2015, Nutrition Resource Services, Inc. issued a voluntary recall of certain Just Be Natural (JBN) and Gifted Nutrition powders containing whey concentrate, whey isolate, casein, and colostrum because they contain undeclared milk.

Recalls & Warnings

7/28/2015

Abnormal Heart Rhythms Linked with Unauthorized Natural Product, Health Canada Warns

On July 27, 2015, Health Canada (the Canadian equivalent of the U.S. FDA) announced that it has received a serious adverse reaction report of abnormal heart rhythms associated with the use of an unauthorized natural product in Canada called Remogen, which contains the drug ibogaine.

Recalls & Warnings

7/12/2015

Marketers of Memory Supplement to Pay $1.4 Million to Settle FTC Charges

On July 8, 2015, the FTC announced the marketers of Procera AVH (Brain Research Labs Inc.) have agreed to pay $1.4 million to settle charges they made deceptive claims that the supplement could significantly improve memory, mood and cognitive function.

Recalls & Warnings

7/02/2015

Maker of Arthritis Supplement Warned for Manufacturing Violations, Drug Claims

On June 17, 2015, the FDA issued a warning letter to Desert Stream, Inc.

Recalls & Warnings

6/17/2015

Maker of Joint Supplement Warned for Manufacturing Violations

On May 29, 2015, the FDA issued a warning letter to Total Health Advanced Nutrition, Inc.

Recalls & Warnings

9/05/2015

Maker of Multivitamin and Fish Oil Warned for Manufacturing Violations

On July 22, 2015, the FDA issued a warning letter to Westar Nutritional Corp. dba Viva Life Science, Inc.

Recalls & Warnings

11/11/2015

Consuming a Single Energy Drink May Increase Cardiovascular Risk

A recently published study found that consumption of a single caffeinated energy drink significantly increased blood pressure and noradrenaline levels in healthy young adults. The researchers noted these changes could potentially increase the risk of cardiovascular events.

Recalls & Warnings

9/26/2015

Seller of Muscle Supplements and More Warned for Manufacturing Violations

On August 14, 2015, the FDA issued a warning letter to Chaotic Labz, Inc.

Recalls & Warnings

9/18/2015

High Levels of Mercury and Lead Found in Ayurvedic Herbal Supplements

On September 17, 2015, the FDA announced that Shree Baidyanath Ayurved Bhawan Ayurvedic dietary supplements were found to contain high levels of lead and/or mercury, which can cause serious health problems.

Recalls & Warnings

2/24/2015

Seller of Heart, Brain and Diabetes Supplements Warned for Drug Claims

On February 6, 2015, the FDA issued a warning letter to LCW, Inc.

Recalls & Warnings

5/26/2015

Skin Measurement Device Used to Select Nutritional Supplements Not Approved for This Use, FDA Warns

On May 8, 2015, the FDA issued a warning letter to ZYTO Technologies, Inc.

Recalls & Warnings

5/23/2015

Seller of Magnesium, Calcium, Silver and More Warned for Manufacturing Violations, Drug Claims

On May 8, 2015, the FDA issued a warning letter to Pick and Pay, Inc.

Recalls & Warnings

5/16/2015

FTC Mails Refund Checks to Nopalea Consumers

On May 15, 2015, the FTC announced it is mailing almost 500,000 checks totaling approximately $3 million to consumers who purchased the cactus-based fruit drink Nopalea (TriVita Inc).

Recalls & Warnings

5/13/2015

Amberen Weight Loss Claims Not Supported by Evidence, Says FTC

On May 12, 2015, the FTC announced it filed a complaint to stop Lunada Biomedical Inc. from advertising that its product Amberen is clinically proven to cause substantial weight loss in women over 40.

Recalls & Warnings

4/29/2015

FDA Targets Weight Loss and Workout Supplements Listing Synthetic Stimulant DMBA

On April 24, 2015, the FDA issued warning letters to sellers of weight loss and workout supplements that list a synthetic, amphetamine-like compound called 1,3-dimethylbutylamine (DMBA) on product labels. 

Recalls & Warnings

1/31/2015

Protein Powder Recalled Due to Food Poisoning Risk

On January 30, 2015, Aloha, Inc. issued a voluntary recall of all packages of Premium Protein powder blends in chocolate and vanilla because they have the potential to be contaminated with Staphylococcus enterotoxin .

Recalls & Warnings

1/31/2015

Maker of Soy and Zinc Warned for Manufacturing Violations

On December 18, 2014, the FDA issued a warning letter to PreMark Health Science, Inc.

Recalls & Warnings

1/27/2015

Seller of Aloe, Sexual Enhancement Supplements and More Warned for Manufacturing Violations, Drug Claims

On January 8, 2015, the FDA issued a warning letter to Aloe Man, Inc., following a facility inspection which found the company's products, including The Aloe Man's Super Bright, Dr. Johnson's Maximum Desire, Dr. Johnson's Body Healer, and Dr.

Recalls & Warnings

1/23/2015

Maker of Vitamin Drinks Warned for Manufacturing Violations

On January 7, 2015, the FDA issued a warning letter to NYSW Beverage Brands, Inc.

Recalls & Warnings

1/21/2015

Smoothie Blends Recalled Due to Potential Listeria Contamination

On January 18, 2015, Inventure Foods, Inc. issued a recall of RADER FARMS Fresh Start Smoothie Blend, Fresh Start Sunrise Refresh Fusion, and Fresh Start Daily Power Fusion, because they have the potential to be contaminated with Listeria monocytogenes.

Recalls & Warnings

1/21/2015

Supplement Maker Ordered to Stop Selling Products

On January 15, 2015, a federal judge ordered a permanent injunction against dietary supplement manufacturer Health One Pharmaceuticals, Inc. which requires the company to stop manufacturing and selling dietary supplements.

Recalls & Warnings

1/17/2015

Maker of Magnesium and Potassium Supplements Warned for Manufacturing Violations

On December 23, 2014, the FDA issued a warning letter to Nutri Spec, Inc.

Recalls & Warnings

12/20/2014

Weight Loss Supplement Recalled

On December 19, 2014, Bethel Nutritional Consulting, Inc. issued a recall of one lot of weight loss supplement SLIM-K Capsules because they were found to contain sibutramine.

Recalls & Warnings

12/20/2014

Company Recalls Second Weight Loss Supplement

On December 19, 2014, Bethel Nutritional Consulting, Inc. issued a recall of one lot of weight loss supplement B-Lipo Capsules because they were found to contain Lorcaserin.

Recalls & Warnings

12/12/2014

Seller of B-12, Zinc, Echinacea and More Warned for Manufacturing Violations and Drug Claims

On November 14, 2014, the FDA issued a warning letter to Scientific Botanicals Company, Inc.

Recalls & Warnings

2/24/2015

Seller of Antioxidant Water, Energy Drops Warned for Manufacturing Violations and Drug Claims

On February 18, 2015, the FDA issued a warning letter to Better Health Lab, Inc.

Recalls & Warnings

6/11/2015

FDA Warns Maker of Fruit Energy Drinks for Drug Claims

On May 19, 2015, the FDA issued a warning letter to CK Management, Inc. following a facility inspection which found statements made on product labels and websites about Whole5, Fruit of the Spirit and ViaViente "whole food" fruit puree energy drinks to be drug claims.

Recalls & Warnings

8/07/2015

Male Enhancement and Weight Loss Supplement Containing Drugs Recalled

On August 6, 2015 Blue Square Market Inc. issued a recall of the following supplements which were found to contain undeclared drugs:

Recalls & Warnings

6/28/2014

Chia Seed Recall Expanded

On June 26, 2014, HEALTH MATTERS AMERICA INC.

Recalls & Warnings

4/16/2014

Weight Loss Supplements Found To Contain Prescription Antidepressant and Other Drugs

On March 7, 2014, the FDA issued a warning letter to Deseo Rebajar Inc. because the company's following weight loss products were found to contain drugs:

Recalls & Warnings

1/09/2014

Four Companies Settle FTC Charges of Deceptive Weight Loss Claims

On January 7, 2014, the Federal Trade Commission (FTC) announced that marketers for four weight loss products have agreed to settlements over charges of deceptive weight loss claims.

Recalls & Warnings

10/24/2012

Manufacturer of Green Tea, Vitamin E, Omega-3 and Cranberry Supplements Warned For Manufacturing Violations, Misbranding and Drug Claims

On October 16, 2012, the FDA issued a warning letter to dietary supplement manufacturer Advanced Nutritional Technology Inc.

Recalls & Warnings

11/02/2012

Manufacturer of Prostate, Inflammation and Cholesterol Supplements Warned For Drug Claims

On October 15, 2012, the FDA issued a warning letter to Ortho Molecular Products, Inc. for making drug claims about the following dietary supplements: Candicid Forte, Inflamma-bLOX, Lipitrol, Mucosagen, Prostatrol Forte, Resvoxitrol, Paracid Forte, VascuPak HTN and Lithium Orotate.

Recalls & Warnings

5/03/2013

Maker of Omega-3, Saw Palmetto, St. John’s Wort Supplements And More Warned For Manufacturing Violations and Drug Claims

On March 19, 2013, the FDA issued a warning letter to Sunset Natural Products Inc.

Recalls & Warnings

3/01/2013

Manufacturer of Joint, Weight Loss, Muscle Supplements and More Warned for Adulteration, Misbranding and Drug Claims

On February 4, 2013, the FDA issued a warning letter to DC Nutrition, Inc.

Recalls & Warnings

2/20/2013

Cold, Flu and Stress Supplement Company Warned For Adulteration, Drug Claims And More

On October 5, 2012, the FDA issued a warning letter to dietary supplement manufacturer Wholistic Herbs, Inc. following a facility inspection which found the company's products, including At-Ease, Morning Calm, Aller-Ban, Stomach Flu, Kold & Koff, Kold Sore, and L.

Recalls & Warnings

8/02/2013

Vitamin B, Vitamin C and Multimineral Supplements Recalled Due To Anabolic Steroid Risk

On July 31, 2013, Purity First Health Products, Inc.

Recalls & Warnings

5/10/2013

Maker of Concentration, Pain, Immune, Cholesterol Supplements Warned For Drug Claims

On April 24, 2013, the FDA issued a warning letter to EuroPharma Co., Inc., following a review of the company's website which found statements made about Calm Kids, CholestCaps, CuraMed 375 mg, CuraMed 750 mg, Curamin, Mental Advantage, Tri-Iodine, and Viragen to be drug claims.

Recalls & Warnings

9/13/2013

Metagenics Warned For Misbranding of Medical Foods and Drug Claims

On August 13, 2013, the FDA issued a warning letter to Metagenics, Inc.

Recalls & Warnings

8/16/2013

Ginkgo, Milk Thistle, Cleanse and Nopal Supplement Maker Warned For Manufacturing Violations, Drug Claims

On July 23, 2013, the FDA issued a warning letter to Natural Products Services, Inc.

Recalls & Warnings

7/27/2012

Prescription and Street Drug Alternatives Found in Male Enhancement, Mood, and Sleep Supplements

On July 10, 2012, the FDA issued a warning letter to Evol Nutrition Associates, Inc. subsequent to a 2011 inspection which found a number of the company's products contained prescription and investigational drugs and were misbranded.

Recalls & Warnings

8/30/2012

Supplement Company Warned For Medical Claims and Misbranding Of Omega-3, CoQ10, Noni Juice And More

On July 12, 2012, the FDA issued a warning letter to Alfa Vitamins Laboratories, Inc.

Recalls & Warnings

7/29/2009

FDA Warns Against Body Building Supplements with Steroid-like Compounds

On July 28, 2009, the U.S. FDA notified the public about new safety information concerning products marketed for body building and increasing muscle mass.

Recalls & Warnings

1/16/2010

Recall of Body Building Supplements Containing Steroids

On January 15, 2010, the Food and Drug Administration (FDA) posted a voluntary recall notice from MuscleMaster.com, Inc. regarding all lots and expiration dates of seventeen dietary supplements sold in 2009 from June 1 and Novemember 17.

Recalls & Warnings

12/22/2005

Health Canada Warns Consumers Not to Take Chaparral

On December 21, 2005, Health Canada (Canada's health ministry) warned consumers not to ingest the herb chaparral in the form of loose leaves, teas, capsules or bulk herbal products because of the risk of liver and kidney problems.

Recalls & Warnings

3/16/2006

Garden of Life, Maker of Primal Defense, Settles FTC Charges

On March 9, 2006, The Federal Trade Commission (FTC) announced that an operation that marketed dietary supplements sold at Whole Foods Market, GNC, the Vitamin Shoppe, and on the Internet settled FTC charges that they made deceptive advertising claims about their supplements.

Recalls & Warnings

12/30/2007

FDA Warns Consumers Not to Use Several "Shangai" Sexual Enhancement Supplements

On December 28, 2007, the U.S. Food and Drug Administration (FDA) advised consumers not to buy or use Super Shangai, Strong Testis, Shangai Ultra, Shangai Ultra X, Lady Shangai, and Shangai Regular, also marketed as Shangai Chaojimengnan, products.

Recalls & Warnings

8/16/2006

Marketers of Diabetes Supplement Banned From Claiming Products Treat or Cure Diseases

On August 10, 2006, the Federal Trade Commission (FTC) announced that an operation selling Chinese herbal supplements is banned from claiming its products treat or cure diseases, to settle FTC charges it violated a previous court order.

Recalls & Warnings

5/10/2007

FDA Warns of Two Supplements Containing Pharmaceutical-like Compounds

On May 10, 2007, the FDA advised consumers not to purchase or use "True Man" or "Energy Max" products promoted and sold as dietary supplements throughout the United States.

Recalls & Warnings

7/29/2008

Recall of Sexual Enhancement Supplements Containing Drug

On July 28, 2008 the U.S. FDA announced that Jack Distribution, LLC and G & N works, Inc. are conducting a voluntary nationwide recall of all lot numbers of the company's supplement products sold under the brand names Rize 2 The Occasion and Rose 4 Her.

Recalls & Warnings

7/28/2008

Seizure of Xiadafil VIP Tablets After Company Refuses Recall

On July 24, 2008, the FDA announced that U.S. Marshals seized nearly $74,000 worth of Xiadafil VIP tablets, Lots 6K029 and 6K209-SEI, distributed by SEI Pharmaceuticals, Inc. of Miami, Fla.

Recalls & Warnings

6/15/2009

Sexual Enhancement Supplement Recalled -- Second Time Found with Drug-like Compound

On June 15, 2009, the U.S. FDA announced that, per its order, Hi-Tech Pharmaceuticals, Inc. is conducting a nationwide voluntary recall of the company's product sold under the name Stamina-Rx.

Recalls & Warnings

2/27/2009

$4 Million Settlement by Supplement Maker for False Claims

On February 26, 2009, the Texas Attorney General announced that an agreement was reached with Mannatech Inc. and its former CEO, Samuel L. Caster, both of which had been charged with orchestrating an unlawful marketing scheme that exaggerated their products’ health benefits.

Recalls & Warnings

1/18/2005

Sellers of “Fat Trapper Plus” and “Exercise in a Bottle” Banned from Advertising Weight-Loss Products

On January 18, 2005, the Federal Trade Commission (FTC)announced that Enforma Natural Products, Inc.

Recalls & Warnings

1/05/2005

Marketers of Brain-Rejuvinating Supplement Settle FTC Charges of False Claims

On January 5, 2005, the U.S. Federal Trade Commission (FTC) announced that a company that heavily advertised an herbal dietary supplement called "Sagee" to the Chinese-language and Vietnamese-language communities had settled FTC charges of making false and unsubstantiated claims for the product.

Recalls & Warnings

6/17/2004

FTC Challenges Deceptive Weight Loss Claims for Supplement Targeted at Hispanics

On June 17, 2004, the Federal Trade Commission (FTC) announced a new law enforcement action challenging false advertising for the 1-2-3 Diet Kit, a purported weight loss product.

Recalls & Warnings

7/30/2003

Maker of Weight-Loss and Cellulite Treatment Ordered to Stop False Claims and Pay Consumer Redress

On July 30, 2003 the Federal Trade Commission (FTC) reported that a Canadian-based company operating in the United States under the name “Bio Lab,” and its president, Jean-Francois Brochu, have agreed to settle FTC charges that they deceived consumers through false and unsubstantiated advertising ...

Recalls & Warnings

5/28/2003

Warning and Recall for "Herbal" Sexual Enhancement Supplement in Canada Illegally Containing Pharmaceutical Compound

On May 27, 2003 - Health Canada warned consumers not to use Hua Fo VIGOR-MAX tablets, a Chinese herbal product that contains tadalafil.

Recalls & Warnings

3/11/2003

Rexall Agrees to Pay up to $12 million to Users of Misleading Cellulite Supplement

On March 11, 2003, the Federal Trade Commission (FTC) reported that Rexall Sundown, Inc. (Rexall) will pay up to $12 million to resolve FTC charges regarding its marketing of the dietary supplement, "Cellasene," a purported cellulite treatment product.