Reviews and Information for Cholestene

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Product Review

Red Yeast Rice Supplements Review

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

Recalls & Warnings

March 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

Protein Powders, Shakes, and Meal Replacements Review

Find Out Which Protein Products Passed or Failed Our Tests

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.

Product Review

CBD Oils, Softgels, Gummies, Creams & Salves Review

See How Much CBD and THC We Found in Products.

CL Answer

My doctor warned me that red yeast rice can cause liver damage - is that true?

Can red yeast rice cause liver damage? More information on its effects, including possible danger to the liver and kidneys.

Product Review

Collagen Supplements Review

See our Top Picks for Wrinkles and Joints

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

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

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

Product Review

Probiotic Supplements Review (Including Pet Probiotics)

Probiotics: See What They Really Contain and Our Top Picks

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.

Product Review

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

Do Creatine and BCAAs Really Improve Strength and Recovery?

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.

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

Bone Broth Review

Find the Best Bone Broth for Quality, Taste, and Value. Four of 10 Products Fail to Get CL Approval.

Product Review

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

Avoid Lead in Greens, Problems with Pills, and Don't Give Up Eating Whole Foods.

Product Review

Iron Supplements Review (Iron Pills, Liquids and Chews)

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

Recalls & Warnings

March 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

Melatonin Supplements Review

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

Product Review

Cranberry Juices and Supplements Review

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

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.

Product Review

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

See Our Omega-3 Top Picks and Avoid Rancid Fish Oils.

Product Review

Vitamin C Supplements Review

Find the Best Vitamin C Supplements

Product Review

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

Some green teas provide barely any green tea polyphenols, while some others are high strength. See the Test Results and Our Top Picks for Green Tea.

Product Review

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

See Our Top Picks and Which 5 Failed Testing

Product Review

Black Seed Oil Review

Find Out Which Black Seed Oil Supplements Passed or Failed Our Tests. See Our Top Picks.

Product Review

Sunflower Seeds and Butters Review

High Levels of Toxin Found in Most Sunflower Seeds and Butters

Product Review

Turmeric and Curcumin Supplements and Spices Review

See Our Top Picks Among Turmeric Products

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.

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.

Product Review

Reishi Mushroom Supplements Review

Find the Best Reishi Mushroom Supplement. See How Reishi Supplements Differ.

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!

Product Review

Lion's Mane and Chaga Supplements Review

Read Labels Carefully -- Many Can Mislead

CL Answer

Where to Safely Buy Real Vitamins and Supplements Online, Not Fakes or Counterfeits

ConsumerLab explains how to avoid counterfeit vitamins and supplements when shopping online on Amazon, Walmart.com, and other sites. Learn to identify authorized sites and sellers and avoid fake supplements. Use the brand-by-brand guide to protect yourself from risk.

Product Review

CoQ10 and Ubiquinol Supplements Review

Find the Best CoQ10 and Ubiquinol Supplements and Learn How They Differ

Product Review

Saffron Supplements Review

See How Saffron Supplements Compare and What They Do

Product Review

Multivitamin and Multimineral Supplements Review

Best Multivitamins -- Caution with Gummies

Product Review

Avocado Oil Review

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

Product Review

L-Arginine Supplements Review

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

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.

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.

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.

Product Review

Elderberry Supplements Review

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

Product Review

Garlic Supplements Review

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

Product Review

Whole, Ground, Milled, and Cracker Flaxseed Review

High Levels of Cadmium Found in Flaxseed Products — Testing Expanded

Product Review

SAMe (S-adenosyl-methionine) Supplements Review

Choose the Best SAMe Supplement and Save Money

Product Review

Quercetin & Rutin Supplements Review

Quality's a Concern With Quercetin and Rutin Supplements -- Only 17% of Claimed Amount In One

Product Review

Alpha-Lipoic Acid Supplements Review

Choose the Best Alpha-Lipoic Acid Supplement — See the Amounts of Active "R-Isomer" We Found

Product Review

Berberine and Goldenseal Supplements Review

Tests Reveal the Best and Worst Berberine and Goldenseal Products

Product Review

Shelled Walnuts (Halves & Pieces)

See Our Top Picks for Walnuts

Product Review

Potassium Supplements Review

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

Recalls & Warnings

August 16, 2023

FDA Warns Sellers of Homeopathic Products for Infants and Children

On August 9, 2023, the FDA issued a warning letter to ALVA-AMCO Pharmacal Companies, LLC and CalmCo LLC, previously named Ketomi LLC, following a review of the company websites, which found statements about company homeopathic products to be drug claims because they are intended to diagnose, cure, ...

Product Review

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

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

Product Review

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

Choose the Best Choline Supplement. Find Out How Much Choline Popular Supplements Really Provide.

Product Review

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

Find the Best Vitamin D Supplement and Avoid Problems

Product Review

Vision Supplements Review (with Lutein, Zeaxanthin & AREDS2 Formulas)

Find the Best Vision Supplement Based Our Tests

Product Review

Zinc Supplements, Lozenges, and Melts Review

Find the Best Zinc Supplements, Including Lozenges for Colds.

CL Answer

Do "Mr. Happy Stack" supplements improve memory, cognition and mood, and are they safe?

Find out if Happy Stack supplements really work to enhance memory and cognition, plus safety and side effects. ConsumerLab.com's answer explains.

Recalls & Warnings

August 20, 2024

Two Sexual Enhancement Supplements Sold on Amazon Recalled

On August 20, 2024, Veata LLC Endurance Pro Energy Boost capsules and Boulla LLC Boom Max capsules were recalled because they contain sildenafil, a prescription medication which is not permitted in dietary supplements.

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

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

18% of Joint Health Supplements Failed to Pass Our Tests. See Which Passed or Failed, and Our Top Picks.

Product Review

DHEA Supplements Review

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

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.

Product Review

Bilberry Supplements Review

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

Recalls & Warnings

September 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

Product Review

Acai Berry Supplements and Beverages Review

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

Product Review

Maca Supplements Review

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

Product Review

Valerian Supplements Review

Choose the Best Valerian Supplement. Strength and Contamination Vary Widely Among Popular Valerian Brands.

Product Review

L-Tryptophan and 5-Hydroxytryptophan (5-HTP) Supplements Review

Choose the Best L-Tryptophan and 5-HTP Supplements. CL Tests Identify High Quality L-Tryptophan and 5-HTP (5-Hydroxy-L-Tryptophan) at the Best Value.

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.

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.

Product Review

Ashwagandha Supplements Review

Find the Best Ashwagandha Supplement. Only 38% of Ashwagandha Products Pass Tests.

Recalls & Warnings

November 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.

News Release

February 26, 2025

ConsumerLab Survey Shows 21 Most Popular Vitamins and Supplements

White Plains, New York, February 26, 2025 — A recent survey of more than 8,400 people who regularly use dietary supplements shows that among the 212 most popular supplements, those that experienced the greatest absolute growth in popularity during 2024 were biotin (+9.

News Release

February 25, 2025

Top-rated Vitamin and Supplement Brands and Merchants for 2025 Based on Consumer Satisfaction

White Plains, New York, February 25, 2025 — Each year, ConsumerLab.com surveys its free e-newsletter subscribers about the vitamins and supplements that they use. The results below are based on over 8,400 responses collected in November/December 2024.

Recalls & Warnings

November 07, 2024

Sexual Enhancement Supplements Sold on Amazon Recalled

On November 4, 2024, four sexual enhancement supplements sold on Amazon and other websites, ZoomMax and ZapMax (Boulla LLC) and VitalityXtra and PeakMax (VitalityVita LLC) were recalled because they were found to contain undeclared prescription drugs, ...

Recalls & Warnings

July 21, 2020

51 CBD Products Recalled Due to Lead Contamination

On June 23, 2020, InHe Manufacturing, LLC and MHR Brands issued a recall of fifty-one CBD products due to contamination and/or potential with lead. Thirty-six of the products are marketed for people and fifteen of the products are marketed for pets.

Product Review

Potassium Iodide (KI) and Iodate (KIO₃) Radioprotective Pills Review

Learn How to Choose the Best Radioprotective Iodine Pill and Use It Properly

Product Review

Huperzine A Supplements Review

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

CL Answer

Should you take olive oil as a supplement?

Although extra virgin olive oil has many possible health benefits, such as reduced risk of heart disease and improved blood sugar control, these and other benefits have been demonstrated when olive oil replaces for saturated fats in the diet, not when taken as a supplement, as we explain.

Recalls & Warnings

June 24, 2024

Canned Coffee Recalled Due to Botulism Risk

On June 17, 2024, Snapchill LLC recalled its canned coffee products because they have the potential to grow the toxic bacterium Clostridium botulinum.

Recalls & Warnings

April 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

November 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

July 14, 2022

FDA Warns Company Selling Supplements with Dangerous Steroid-like Substances

On July 6, 2022, the FDA issued a warning letter to Elite Supplement Center LLC and Elite Supplement Training Facility LLC for selling the following products labeled as containing steroid-like substances known as selective androgen receptor modulators (SARMs), which are not permitted in dietary ...

Recalls & Warnings

July 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.

CL Answer

What are the side effects of red yeast rice?

Find out which side effects can be caused by red yeast rice supplements that are taken to lower cholesterol levels. ConsumerLab.com's answer explains.

Recalls & Warnings

April 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

July 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

November 18, 2024

Manufacturer of Grandma’s Herbs Kidney Warned by FDA

On October 20, 2023, the FDA issued a warning letter to Top Health Manufacturing, LLC, manufacturer of Grandma’s Herbs Kidney supplement, following an inspection of the company’s facility that found its products to be adulterated because they were, packed, labeled or held under ...

Recalls & Warnings

September 24, 2024

Manufacturer of Mushroom Gummies Warned by FDA for Violations

On August 13, 2024, the FDA issued a Warning Letter to Restorative Botanicals, LLC, following an inspection of the company’s facility found the company’s products, including its My GUT Shrooms Gummies and My IMMUNE Shrooms Capsules, to be adulterated because they were prepared, ...

Recalls & Warnings

February 03, 2025

Four Male Enhancement and Energy Supplements Found to Contain Drugs

On January 16, 2025, the FDA issued a Warning Letter to Mihon Corp. d/b/a VitalityVita and Boulla, LLC after FDA analysis found four of the company’s supplements, VitalityXtra, PeakMax, ZapMax, and ZoomMax, to contain undeclared sildenafil.

Recalls & Warnings

April 23, 2025

FDA Warns Consumers Not to Use ADVANCED KING Joint Supplement

On February 10, 2025, the FDA warned consumers not to purchase or use the joint pain supplement ADVANCED KING (Naturista Store LLC), because FDA analysis confirmed the product contains dexamethasone, diclofenac, and methocarbamol.

News Release

February 26, 2024

Latest ConsumerLab Survey Shows Growth in Popularity of Magnesium and Several Smaller Supplements

White Plains, New York, February 26, 2024 — A recent survey of more than 10,000 people who regularly use dietary supplements shows that supplements that experienced the greatest absolute growth in popularity during 2023 were pregnenolone (+7.5 percentage points), magnesium (+4.8 pts), berberine (+4.

News Release

February 25, 2024

Top-rated Vitamin and Supplement Brands and Merchants for 2024 Based on Consumer Satisfaction

White Plains, New York, February 25, 2024 — Each year, ConsumerLab.com surveys its free e-newsletter subscribers about the vitamins and supplements that they use. The results below are based on over 10,000 responses collected in November/December 2023.

News Release

February 25, 2023

Top-rated Vitamin and Supplement Brands and Merchants for 2023 Based on Consumer Satisfaction

White Plains, New York, February 25, 2023 — Each year, ConsumerLab.com surveys its free e-newsletter subscribers about the vitamins and supplements that they use. The results below are based on 8,600 responses collected in November/December 2022.

News Release

February 24, 2023

Probiotics Rise in Popularity as Vitamin C, Melatonin, and Others Dip in Latest ConsumerLab Survey of Supplement Users

White Plains, New York, February 25, 2023 —A recent survey of 8,600 people who regularly use dietary supplements shows that probiotics (+3.04 percentage points), quercetin (+2.3 pts), and vitamin K (+1.

News Release

May 26, 2022

50% of Red Yeast Rice Supplements Fail ConsumerLab Tests

  White Plains, New York, May 26, 2022 — Red yeast rice naturally contains cholesterol-lowering lovastatin compounds. However, recent ConsumerLab tests of popular red yeast rice products on the market revealed many did not contain any detectable lovastatin.

News Release

February 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.

CL Answer

What are the health benefits of tart cherry juice?

See the evidence for tart cherry juice health benefits from clinical studies. Find out if tart cherry has anti-inflammatory effects, if it can improve sleep, lower high blood pressure, or help for muscle pain and osteoarthritis.

Recalls & Warnings

December 26, 2023

Total Body Nutrition, TBN Labs, and Loud Muscle Science Agree to Stop Selling Adulterated and Misbranded Dietary Supplements

On December 13, 2023, Total Body Nutrition LLC, TBN Labs LLC, and Loud Muscle Science LLC, as well as the companies’ owner, Mohammed Islam, agreed to stop manufacturing and distributing adulterated and misbranded dietary supplements and to comply with dietary supplement current good ...

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.

Recalls & Warnings

May 12, 2020

FTC Halts Deceptive Supplements & Cosmetics "Free Trial" Scheme

On May 8, 2020, the owners of AH Media Group, LLC agreed to halt their allegedly deceptive practice of luring consumers with supposed "free trial" offers for cosmetics and dietary supplements, then enrolling them in subscriptions and billing them without their consent.

Recalls & Warnings

April 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

August 16, 2023

FDA Warns Hekma Center, LLC for Promoting Products to Treat Anemia, Diabetes, Depression, & More

On June 2, 2023, the FDA issued a warning letter to Hekma Center, LLC following review of the company’s website and social media, which found statements about the company’s Natural Supplements for Anemia, Lymf (Galium aparine), Natural Supplements for Cardiomyopathy, Magic1 (Moringa ...

Recalls & Warnings

April 10, 2025

MTM OPS Men’s Multivitamin Recalled

On April 9, 2025, MTN OPS, LLC recalled 7,546 bottles of MTN OPS MULTI-V Men's Daily Multivitamin dietary supplement because it contains undeclared soy flour.

Recalls & Warnings

December 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

April 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

April 02, 2021

FDA Warns Sellers of Prostate, Reishi, Immune Products, and More

On March 16, 2021, the FDA issued warning letters to two companies following reviews of their websites which found statements made about the companies' products to be drug claims.

Recalls & Warnings

April 02, 2021

Three Male Enhancement Products Recalled Due to Undeclared Drugs

Between March 24 and 26, 2021, three companies issued recalls of their male enhancement capsules because FDA analysis found them to contain sildenafil and tadalafil.

Recalls & Warnings

January 11, 2023

Male Sexual Enhancement Supplement Found to Contain Prescription Drug

On January 9, 2022, the FDA issued a warning letter to Distributor RFR, LLC after laboratory analysis of the company’s SANGTER Natural Male Energy Supplement found the product to contain undeclared sildenafil, a prescription medication.

Recalls & Warnings

November 28, 2022

Seller of Elderberry, Tea Warned for Claims of Treating Cold, Flu, Cancer

On October 18, 2022, the FDA issued a warning letter to Rosebud’s Ranch and Garden, LLC after inspection of the company’s website and social media found statements about the company’s Domestic Divas – Colds and Flu (Tea), Domestic Divas - No Pain No Gain Tea, Green ...

Recalls & Warnings

December 12, 2022

FDA Warns Saffron USA for Promoting Teas to Treat Insomnia, Osteoporosis & Cancer

On September 23, 2022, the FDA issued a warning letter to Saffron USA LLC following inspection of the company’s website which found statements about its Allergy Blend, Chamomile Tea Petals, Diabetic Support Blend, Orange Blast Tea, and Saffron Loose Tea products to be drug ...

Recalls & Warnings

January 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

August 03, 2022

Sexual Enhancement Supplement Recalled Due to Sildenafil

On August 1, 2022, DISTRIBUTOR RFR, LLC recalled one lot of SANGTER Energy Supplement 3000 mg to the consumer level after FDA analysis found the product to contain undeclared sildenafil, a prescription medication.

Recalls & Warnings

September 29, 2022

Sexual Enhancement Supplement Sold on Amazon and Walmart Recalled Due to Undeclared Drugs

On September 27, 2022, Proper Trade LLC/My Stellar Lifestyle recalled two lots of Wonder Pill after Amazon laboratory analysis found the product to contain undeclared tadalafil, a prescription medication.

Recalls & Warnings

August 08, 2022

Seller of CBD Warned for COVID-19 Claims

On August 4, 2022, the FDA sent a warning letter to FluxxLab LLC following a review of the company’s website and social media which found statements about the company’s Covid-19 Immune Support Tincture and CBDA+CBD Oil Tincture products to be drug claims because they ...

Recalls & Warnings

September 01, 2022

FDA Warns Elderberry Fair & Co for Promoting Elderberry Supplements and Apple Cider to Treat Colds & Flu

On August 15, 2022, the FDA issued a warning letter to The Elderberry Fairy & Co., LLC after review of the company’s website found statements about the company’s Elderberry Syrup with Honey, Elderberry Syrup with Agave, and Organic Fire Cider to be drug claims.

Recalls & Warnings

July 13, 2022

FDA Warns Sellers of Tainted Honey-Based Sexual Enhancement Products

On July 12, 2022, the FDA issued warning letters to four companies selling honey-based products promoted for sexual enhancement after tests conducted by the FDA found the products to contain the prescription drugs Tadalafil and Sildenafil.

Recalls & Warnings

February 13, 2019

Supplements Promoted for Alzheimer's Disease and Dementia Sell "False Hope," Warns FDA

On February 11, 2019, the FDA warned consumers to beware supplements promoted to prevent or treat Alzheimer's disease or dementia.

Recalls & Warnings

May 11, 2006

Weight-Loss Marketers Pay $3 Million for Deceptive Advertising

On May 11, the Federal Trade Commission (FTC) announced that sellers making questionable weight-loss and fat-loss claims to peddle skin gels and diet supplements will pay $3 million to settle charges that their deceptive claims violated federal law.

Recalls & Warnings

March 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

September 01, 2020

Custom Nutraceuticals, LLC Warned for Manufacturing Violations

On August 6, 2020, the FDA issued a warning letter to Custom Nutraceuticals, LLC, following a facility inspection which found the company's products, including Thermal Revolution Black, Anabolic Blackout Raspberry Lemonade, Militia Re-COMP, and Rhino Rampage Wildberry to be ...

Recalls & Warnings

December 15, 2020

FDA Warns JC Ayur Life LLC for Drug Claims

On October 29, 2020, the FDA issued a warning letter to JC Ayur Life LLC following a review of the company's website, which found statements made about the company's product Heritage of Ayurveda Dia-Tonic Incudil Herbal Dietary Supplement to be drug claims.

Recalls & Warnings

November 20, 2020

FTC Files Complaint Against Two Supplement Companies for Deceptive Marketing

On November 20, 2020, the FTC approved a Part 3 administrative complaint against Health Research Laboratories, LLC, its owner Kramer Duhon, and Whole Body Supplements, LLC for making unverified claims that their products can prevent or treat diseases.

Recalls & Warnings

November 30, 2023

Discover Health, LLC Warned for Promoting CBD Products for Cancer, Epilepsy, & More

On November 16, 2023, the FDA issued a Warning Letter to Discover Health, LLC d/b/a Discover CBD and Strain Snobs following a review of the company’s websites that found statements about the company’s Active CBD Oil – Full Spectrum Distillate Cartridge, Active CBD Oil – ...

CL Answer

Where to Safely Buy Real Water Filters Online, Not Fakes or Counterfeits

ConsumerLab explains how to avoid counterfeit water filters when shopping online on Amazon, Walmart.com, and other sites. Learn to identify authorized sites and sellers and avoid fake filters. Use the brand-by-brand guide to protect yourself from risk.

CL Answer

When taking a statin drug like Lipitor or Crestor, are there supplements I should avoid or take?

Learn about the interactions between certain supplements and atorvastatin (Lipitor), rosuvastatin (Crestor), and other cholesterol-lowering statins.

Recalls & Warnings

February 09, 2022

FDA Warns Seller of Colloidal Silver Eye Drops, Copper Products & More

On February 1, 2022, the FDA issued a warning letter to New Earth Healing Essentials, LLC d/b/a 5D Full Disclosure following a review of the company’s website, which found statements made about some of the company's products, including Plasma Colloidal Silver Eyedrops, Gaia’s ...

Recalls & Warnings

January 13, 2022

Senna Laxative Recalled Due to Microbial Contamination

On January 11, 2022, Lohxa LLC issued a voluntary recall of one lot of Senna Syrup 8.

Recalls & Warnings

April 17, 2020

Joint Pain Supplement Isoprex Settles Charges of Making False Claims

On April 16, 2020, Renaissance Health Publishing, LLC, agreed to halt their allegedly deceptive advertising claims about their Isoprex supplement that targeted older consumers nationwide after the Federal Trade Commission (FTC) filed a complaint.

Recalls & Warnings

April 14, 2020

FTC Warns Companies Selling Immune "Boosters," Vitamin C and More for Coronavirus Claims

On April 14, 2020, the FTC announced that it has sent warning letters to ten companies for selling products such as immune boosters, silicone facial brushes, air purifiers, and intravenous vitamin C with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

November 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

December 05, 2024

Liquid Multivitamin Recalled

On November 6, 2024, Armonia Natural Store LLC issued a recall of 64 bottles of OneMultivitaminic GAF-PLUS Advance 300 ml because they contain undeclared acetaminophen and dexamethasone phosphate (which are not permitted in dietary supplements) and the undeclared sweetener aspartame.

Recalls & Warnings

December 19, 2024

Toxic Herb Found in More Weight Loss Supplements

On December 13, 2024, Motivate Me Ashley, LLC recalled the following VidaSlim brand products: VidaSlim 90-day (Original Root, Root Plus, and Root Capsules), VidaSlim 30-day (Original Root, Root Plus, and Root Capsules), VidaSlim 7-day Sample Size (Original Root, Root Plus, and ...

Recalls & Warnings

September 12, 2024

Root Bioscience Warned for CBD Claims

On August 30, 2024, the FDA issued a warning letter to Root Bioscience Brands, LLC dba Naternal following a review of the company's websites, which found statements made about the company's products, including CBD Oils Move CBD+CBG Oil, Rest CBD+CBN Oil, Nurture Broad Spectrum ...

Recalls & Warnings

September 23, 2024

Lactaid Milk Recalled Due to Allergen

On September 20, 2024, HP Hood LLC voluntarily recalled five SKUs of refrigerated Lactaid Milk due to the product potentially containing trace amounts of almond, which is not declared on the label. No illness has been reported to date.

Recalls & Warnings

September 24, 2024

Supplement for Eczema Recalled

On September 18, 2024, 123Herbals LLC issued a recall for all lots of Vail-Bon Jie Yang Wan capsules, which are promoted to treat eczema and other skin conditions, because they contain undeclared dexamethasone and chlorpheniramine.

Recalls & Warnings

February 27, 2025

Male Enhancement Supplement Sold on Amazon and Walmart Recalled

On February 25, 2025, Natural Dior LLC recalled affected lots of a dietary supplement Vitafer-L Gold Liquid because it contains undeclared tadalafil, which is not permitted in dietary supplements.

Recalls & Warnings

March 10, 2025

Probiotics and Prebiotic Gummies Recalled

On January 17, 2025, Health and Happiness (H&H) LLC.

Recalls & Warnings

March 13, 2025

FTC Sends Refund Checks to Consumers of Pure Green Coffee Supplement

On March 6, 2025, the Federal Trade Commission (FTC) announced it is mailing 39,977 checks totaling more than $905,000 to consumers who purchased Pure Green Coffee, to settle charges the product was promoted with deceptive health claims and marketing practices.

Recalls & Warnings

May 06, 2025

Joint Supplement Recalled Due to Salmonella Risk

On April 15, 2025, Optimal Carnivore, LLC recalled 1,483 bottles of Bone & Joint Restore capsules because they have the potential to be contaminated with Salmonella.

Recalls & Warnings

June 09, 2025

GNC Women's 30+ Vitapak Recalled

On April 25, 2025, GNC Holdings LLC recalled 144,430 units of GNC Women's 30+ Vitapak, Carton of 30 Sachets, because they contain an undeclared fish allergen (parvalbumin).

Recalls & Warnings

April 03, 2024

FDA Warns Ambaya Gold for Promoting Products for Depression, Cancer, & Arthritis

On December 5, 2023, the FDA issued a Warning Letter to Ambaya Gold Health Products, LLC following review of the company’s website and social media, which found statements about the company’s Brain Balance, Immune System Boost, Dentist In A Bottle, Essensiac, Fulvic Green, Silver ...

News Release

February 24, 2022

Consumers Returned to Pre-Pandemic Supplement Usage in 2021, ConsumerLab Survey Reveals

White Plains, New York, February 24, 2022 —A survey of 8,049 people who use dietary supplements shows many supplements that declined in use in 2020 began bouncing back in 2021, such as magnesium (+2.4 percentage points), and CoQ10 (+2.7 pts).

Recalls & Warnings

October 12, 2020

NutraClick to Pay $1.04 Million for Illegally Billing Consumers

On September 22, 2020, the Federal Trade Commission (FTC) announced that NutraClick LLC agreed to pay $1.04 million to settle FTC charges that the company was deceptively selling and billing consumers for supplements and beauty products.

Recalls & Warnings

January 15, 2024

Suprex Carb & Sugar Block Recalled

On December 7, 2023, Vita 360, LLC issued a recall of one lot of SUPREX Plant Based Nutrition Carb & Sugar Block after FDA analysis found it to contain only 16 mcg of chromium per serving and not 100 mcg of chromium per serving, as listed on the label.

Recalls & Warnings

January 15, 2024

5 Star Nutrition Will Pay $4.5 Million for Selling Misbranded Workout Supplements

On January 12, 2024, Defyned Brands, also known as 5 Star Nutrition LLC, pleaded guilty in federal court to three-counts of distributing misbranded dietary supplements following an investigation by the Food and Drug Administration’s Office of Criminal Investigations (FDA-OCI).

Recalls & Warnings

October 09, 2023

Orgain Protein Powder Recalled Due to Allergen Risk

On October 4, 2023, Orgain LLC issued a recall of four lots of the company’s Organic Protein Powder + Superfoods, Creamy Chocolate Fudge flavor protein powder after a co-manufacturer informed the company that the product contained undeclared sesame, which is now one of nine food ...

Recalls & Warnings

April 17, 2024

FDA Warns Lipari Foods for Mislabeled Walnuts, Other Violations

On April 9, 2024, the FDA issued a Warning Letter to Lipari Foods Operating Company, LLC following multiple complaints and subsequent product recalls in August and September of 2023, which found the company did not follow the requirements of Current Good Manufacturing Practice (CGMP), Hazard ...

Recalls & Warnings

April 24, 2024

Organic Basil Sold at Trader Joe’s & Other Markets Recalled Due to Salmonella Risk

On April 18, 2024, Infinite Herbs, LLC issued a recall of certain packages of Infinite Herbs and Melissa’s brand fresh organic basil due to the potential presence of Salmonella.

Recalls & Warnings

November 09, 2023

Zazzee Naturals Warned for MSM Eye Drop Claims

On October 30, 2023, the FDA issued a Warning Letter to Dexterity Health, LLC DBA Zazzee Naturals following review of the company’s Amazon storefront, which found statements about the company’s Liquid MSM Drops to be drug claims.

Recalls & Warnings

November 30, 2023

Original The Rock Capsules Recalled Due to Undeclared Sildenafil

On October 18, 2023, Noah’s Wholesale, LLC issued a nationwide recall of one lot of the company’s Original The Rock capsules after FDA analysis found the product to contain undeclared sildenafil, a prescription medication.

Recalls & Warnings

July 24, 2023

ONO Overnight Oats Recalled Due to Allergen Risk

On July 18, 2023, ONO LLC issued a voluntary recall of the company’s ONO Vegan Blueberry Muffin Protein Overnight Oats due to undeclared milk.

Recalls & Warnings

August 03, 2023

Ozona Organics Liquid Probiotics Recalled Due to Risk of Microbial Contamination

On August 1, 2023, Ozona Organics, LLC recalled certain lots of its probiotic supplement, Ozona Probiotics for Digestive Health, also labeled as GoHealthy Probiotics for Infants, Toddlers, and Kids and GoHealthy Probiotics for Infants, Kids, Men, and Women, due to the ...

Recalls & Warnings

December 22, 2021

FDA Warns Seller of Liquid Magnesium, B-12, Berberine & More

On December 9, 2021, the FDA issued a warning letter to Wholly Liquid Nutritional Supplements LLC because it found statements on the company's website and social media about its products, including SpiroLaze, BioLaze, LiquiLaurin, VIT-B12, DeStress, and Omega Plus, to be ...

Recalls & Warnings

December 09, 2021

FDA Warns Seller of Curcumin, Lion's Mane, Quercetin & More

On November 9, 2021, the FDA issued a warning letter to Synaptent, LLC because it found statements on the company's website about its products, including Berberine HCL, Curcumin, Lion's Man, Milk Thistle, Quercetin, Boswellia Serrata Extract, and Garlic Extract to be ...

Recalls & Warnings

January 04, 2024

Toxic Herb Found in More Tejocote Root Supplements

On January 3, 2024, the FDA warned consumers not to purchase or use certain tejocote root supplements after FDA laboratory analysis confirmed the products contain yellow oleander (Thevetia peruviana), a toxic herb.

News Release

February 26, 2021

COVID Changed Supplement Popularity in 2020, ConsumerLab Survey Reveals

White Plains, New York, February 26, 2021 — A survey of 9,647 people who use dietary supplements shows that the supplements which experienced the greatest growth in popularity in 2020 were those being promoted to prevent or treat infection with SARS-CoV-2, the coronavirus that causes COVID-19.

News Release

February 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.

News Release

March 03, 2020

Best and Worst Chia Seed Products Revealed by ConsumerLab

White Plains, New York, March 3, 2020 — Chia seeds are rich in fiber and a good source of healthful oils, particularly the omega-3 fatty acid ALA (alpha-linolenic acid), as well certain vitamins and minerals.

Recalls & Warnings

April 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.

Recalls & Warnings

September 04, 2018

Federal Court Shuts Down Maker of Sexual Enhancement Products

On August 30, 2018, the FDA announced that U.S.

Recalls & Warnings

November 03, 2022

Seller of CBD Warned for COVID-19 Claims

On November 1, 2022, the FDA issued a warning letter to Alternative Health Distribution LLC (d/b/a CannaAid) following a review of the company’s website, which found statements about the company’s cannabidiol (CBD) products to be drug claims.

Recalls & Warnings

November 10, 2022

Adam’s Polishes Hand Sanitizer Recalled Due to Toxic Methanol

On November 5, 2022, Adam’s Polishes, LLC issued a nationwide recall of 20 lots of Adam’s Polishes Hand Sanitizer following FDA testing, which found the presence of methanol in one lot.

Recalls & Warnings

November 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

January 26, 2023

Allergy Bee Nasal Swabs Contaminated With Illness-Causing Bacteria

On January 18, 2023, the FDA issued a warning letter to Buzzagogo, LLC, after the company’s Allergy Bee Gone for Kids nasal swab products were found to be contaminated with bacteria that have the potential to cause life-threatening illness.

Recalls & Warnings

January 31, 2023

Over $973,000 Returned to NutraClick Consumers

On January 25, 2023, the FTC announced it will be returning over $973,000 to over 17,000 consumers who lost money after NutraClick LLC allegedly automatically enrolled them in unwanted membership programs for supplements and beauty products.

Recalls & Warnings

December 19, 2022

High Impact Plant Protein Powder Recalled

On December 15, 2022, THGH Partners LLC issued a recall of one lot of its High Impact Plant Protein due to the presence of undeclared milk.

Recalls & Warnings

March 22, 2023

Of Concern: The Daily Post and Hiya

White Plains, New York, March 22, 2023 — An "advertorial" for Hiya Kids Daily Multivitamin appearing on the website "The Daily Post" provided misinformation and suggested that ConsumerLab.com recommended this product, which is completely false.

Recalls & Warnings

April 03, 2023

Smoked Salmon Recalled Due to Listeria Risk

On March 14, 2023, Seven Seas International USA, LLC issued a voluntary recall of 295 cases of Biltmore Smoked Sockeye Salmon after routine testing by the Florida Department of Agriculture and Consumer Services discovered the presence of Listeria monocytogenes or Salmonella.

Recalls & Warnings

July 06, 2022

Two Companies Banned From Selling Supplements to Treat Heart Disease, Neuropathy

On June 30, 2022, the Federal Trade Commission (FTC) finalized an administrative complaint order against two Texas-based companies, Health Research Laboratories, LLC and Whole Body Supplements, LLC, for making unverified claims that their products can prevent or treat disease.

Recalls & Warnings

July 26, 2022

Sexual Enhancement Supplement Sold on Amazon Recalled

On July 21, 2022, Ultra Supplements LLC issued a recall of one lot of Sustango capsules after Amazon laboratory analysis found the presence of the prescription drug Tadalafil. The company has received no reports of adverse effects related to this recall to date.

News Release

February 29, 2020

Collagen and Magnesium Rise in Popularity, as Fish Oil and Curcumin Dip in Latest ConsumerLab Survey of Supplement Users

White Plains, New York, February 29, 2020 — A recent survey of 9,782 people who use dietary supplements shows that collagen (+ 4.1 percentage points), magnesium (+ 2.3 pts) and CBD (+ 2.

News Release

February 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.

Recalls & Warnings

April 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

June 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

May 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

April 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).

Recalls & Warnings

December 29, 2020

FDA Warns Five Sellers of CBD for Claims of Treating Arthritis, Alzheimer's and More

On December 22, 2020, the FDA issued warning letters to five sellers of CBD following reviews of the companies' websites, which found statements made about the companies' products to be drug claims.

Recalls & Warnings

September 08, 2020

FDA Warns Seller of Opioid Withdrawal Supplement

On August 25, 2020, the FDA issued a warning letter to Renewal Supplements LLC following a review of the company's website, which found statements made about the company product Opi-Cure to be drug claims.

Recalls & Warnings

December 07, 2023

Belmont Eyecare Warned for Colloidal Silver, MSM, and Castor Oil Eye Drop Claims

On December 1, 2023, the FDA issued a Warning Letter to Belmont Eyecare LLC, following a review of the company’s website, which found statements about the company’s Colloidal Silver Eye Drops, MSM Eye Drops, Organic Daytime Oil Eye Drops, Organic Daytime Oil Eye Drops Small, Organic ...

News Release

August 22, 2019

Best Reishi Mushroom Supplements Identified by ConsumerLab

White Plains, New York, August 22, 2019 — Reishi mushroom supplements are promoted for many uses, from strengthening the immune system and lowering blood sugar, to improving cardiovascular health and reducing cancerous tumors.

News Release

July 31, 2019

ConsumerLab Tests Reveal Best CoQ10 and Ubiquinol Supplements

White Plains, New York, July 31, 2019 — CoQ10 is among the most popular supplements, commonly taken to offset a decline in natural levels of CoQ10 that can occur with the use of statin medications, decrease statin side effects, and increase energy.

News Release

July 10, 2019

Best Selenium Supplements Identified by ConsumerLab

White Plains, New York, July 10, 2019 — Selenium is an essential mineral important for proper immune and thyroid function but taking a selenium supplement is often not necessary and, in some people, may increase the risk of cancer or diabetes.

News Release

June 25, 2019

ConsumerLab Tests Reveal Best B Vitamin Supplements -- 19% of B Vitamin Supplements Fail CL's Tests of Quality

White Plains, New York, June 25, 2019 — B vitamins and complexes are among the most popular supplements sold in the U.S. because B vitamins are essential for a wide range of functions in the body.

News Release

May 15, 2019

ConsumerLab Tests Reveal Big Differences in Digestive Enzyme Supplements

White Plains, New York, May 15, 2019 — Digestive enzyme supplements can help improve digestion and the absorption of nutrients, and may reduce symptoms of indigestion. But to work, they must provide a certain amount of enzyme activity.

News Release

April 25, 2019

Best Coconut Water? ConsumerLab Tests Popular Products, Reveals Top Pick

White Plains, New York, April 25, 2019 — Coconut water is often promoted as a healthy way to stay hydrated and a natural alternative to sports drinks.

News Release

April 01, 2019

Not All Quercetin Supplements Contain What They Claim, ConsumerLab Tests Reveal

White Plains, New York, April 1, 2019 — Quercetin is a flavonoid found in foods such as onions, kale and apples. Sold as a supplement, quercetin is promoted to help with a range of conditions including prostatitis, asthma, and rheumatoid arthritis, as well as blood sugar control.

News Release

March 11, 2019

Best NAC (N-acetyl cysteine) Supplements Identified by ConsumerLab

White Plains, New York, March 11, 2019 — NAC (N-acetyl cysteine) supplements are promoted for many uses, including "liver support," "immune support," and reducing symptoms of the flu and flare-ups of chronic bronchitis.

News Release

March 07, 2019

Best Coconut and MCT Oils Identified by ConsumerLab

White Plains, New York, March 7, 2019 — Coconut oil is often promoted as a "healthy fat" and an alternative source of energy to help with weight loss and in conditions such as Alzheimer's disease because it contains medium chain triglycerides (MCTs).

News Release

February 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

August 24, 2018

Few Red Yeast Rice Supplements Provide Enough Cholesterol-Lowering Compounds to Likely Be Effective, ConsumerLab Tests Reveal

White Plains, New York, August 24, 2018 — Research shows that red yeast rice, which contains naturally-occurring lovastatin compounds, can lower "bad" LDL cholesterol.

News Release

February 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

May 23, 2011

Red yeast rice supplements weaker now than in 2008; Wide variation among brands and contamination discovered by ConsumerLab.com -- Popular cholesterol-lowering supplements tested and compared

WHITE PLAINS, NEW YORK — MAY 23, 2011 — ConsumerLab.com announced today that tests of eleven red yeast rice supplements revealed enormous differences in levels of cholesterol-lowering statin compounds. Statin levels fell dramatically among brands previously tested in 2008.

News Release

July 01, 2008

Tests of ten red yeast rice supplements by ConsumerLab.com reveal significant statin levels, but some pills contaminated -- Popular cholesterol-lowering supplements compared in new report

WHITE PLAINS, NEW YORK — JULY 1, 2008 — ConsumerLab.

Recalls & Warnings

April 27, 2022

FDA Warns Manufacturer of Topical Antiseptic Products for COVID Claims

On April 19th, 2022, the FDA issued a warning letter to Kleenhanz, LLC following a review of the company’s website and social media which found statements about the company’s Kleenhanz Towelettes topical antiseptic products to be drug claims.

Recalls & Warnings

June 30, 2022

FDA Warns Seller of Vision and Allergy Supplements

On May 26, 2022, the FDA issued a warning letter to Golden Lab LLC following an inspection of the website, which found statements about the company’s DoctoRx’s Optimal Formula Ocular Pressure & Optic Nerve Support Formula Ocular Health Capsule, DoctoRx’s Optimal Formula ...

Recalls & Warnings

July 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

July 06, 2021

CBD Products Were Promoted to Treat Cancer and Alzheimer's Without Proof, Says FTC

On July 6, 2021, the Federal Trade Commission (FTC) announced that it has approved a final administrative consent orders against Kushly Industries LLC and the company's owner, Cody Alt, for allegedly making unsupported health claims about its CBD products.

Recalls & Warnings

December 09, 2021

Florida Man Convicted for Distributing Steroids Labeled as Dietary Supplements

On December 9, 2021, 37-year-old Florida resident James Boccuzzi was convicted of one count of conspiracy to defraud the U.S. Food and Drug Administration (FDA) and one count of conspiracy to distribute controlled substances.

Recalls & Warnings

November 09, 2021

Five Brands of Protein Supplements Recalled Due to Allergen Risk

On November 9, 2021, Nutracap Holdings, LLC issued a recall of certain Boba Origin, Etedream, RAW, Steel, and Vital Force protein supplements because they contain potential allergens, including soy, milk, wheat, and/or coconut, that are not declared on the label.

Recalls & Warnings

September 14, 2021

Seller of Lion's Mane, Other Mushroom Supplements Warned by FDA

On July 20, 2021, the FDA issued a warning letter to Brilliant Enterprises LLC because it found statements made on the company's website and social media about mushroom supplements, including Lion's Mane, BoomChaga, CordaCex, and LVL:MAX to be drug claims.

Recalls & Warnings

August 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

August 08, 2022

Recall of Oral Magnesium Laxatives Expanded

On August 3, 2022, Plastikon Healthcare, LLC issued a recall of multiple oral suspension products due to microbial contamination.

Recalls & Warnings

September 28, 2022

FDA Warns Muscle Sports for Joint Health, Immune & Workout Supplement, Vitamin C, Elderberry, and Other Claims

On September 23, 2022, the FDA issued a warning letter to Muscle Sports Products, LLC following inspection of the company’s websites which found statements about company products, including Join Revolution Capsules, IMMUNITY + Powder, Rhino Rampage PUMPED Capsules, Attack Pre-Workout ...

Recalls & Warnings

July 18, 2022

CVS, Target, Walgreens, and Other Oral Magnesium Citrate Laxatives Recalled Due to Bacterial Contamination

On July 14, 2022, Magnesium Citrate Laxative Oral Solution Lemon Flavor products manufactured by Vi-Jon, LLC and sold under various store brand names were recalled after testing identified the presence of the bacteria Gluconacetobacter liquefaciens.

Recalls & Warnings

June 16, 2004

Ads for Various Diet Pills and Topical Gels Don’t Cut the Fat, Says the FTC

On June 16, 2004, The Federal Trade Commission (FTC)charged a Utah-based company, five related corporations, and three individuals operating as a common enterprise with making numerous false and unsubstantiated claims for weight-loss and fat-loss gels and supplements.

Recalls & Warnings

May 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

September 14, 2023

FDA Warns CVS, Walgreens, Similasan & Others for Eye Drop Violations

On September 11, 2023, the FDA issued Warning Letters to the following eight sellers of homeopathic and other types of eye drops regarding the products noted in italics due to a variety of violations of FDA regulations, most notably that they were marked with claims suggesting that they could cure, ...

News Release

December 20, 2004

Testing of Alpha-lipoic acid supplements by ConsumerLab.com finds most meet label claims but one with only 15% of ingredient — Antioxidant of potential benefit in diabetes and other conditions

WHITE PLAINS, NY — December 20, 2004 — ConsumerLab.com announced today that one of 21 alpha-lipoic acid supplements recently tested contained only 15% of the alpha-lipoic acid that it claimed. Alpha-lipoic acid is an antioxidant naturally produced in the body.

News Release

July 07, 2004

ConsumerLab.com finds several herbal sleep supplements fail tests for quality — Results for 13 valerian products released today

WHITE PLAINS, NY — Wednesday, July 7, 2004 — ConsumerLab.com announced today that five valerian dietary supplements failed to pass recent testing due to low potency and/or contamination. Valerian, an herbal sleep aid, accounted for $47 million in sales in the U.S.

Recalls & Warnings

March 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

February 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

April 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

September 05, 2020

Bio aaa Advance Hand Sanitizer Recalled

On September 3, 2020, AJR Trading LLC recalled one lot of bio aaa Advance Hand Sanitizer because different lots of the product may contain methanol, which is toxic when absorbed through the skin or ingested.

Recalls & Warnings

September 03, 2020

Red-E Male Enhancement Capsule Recalled

On September 1, 2020, The Protein Shoppe, LLC issued a recall of Red-E male enhancement capsules because FDA analysis found it to contain sildenafil.

Recalls & Warnings

September 15, 2020

FDA Warns Seller of Unapproved "COVID-19 test package"

On June 29, 2020, the FDA issued a warning letter to Pomegranate Consulting, LLC, Pomegranate Consulting, Ltd. dba Glorious One-Pot Meals for selling COVID-19 test package, an unapproved, adulterated, and misbranded antibody test for coronavirus (COVID-19).

Recalls & Warnings

September 11, 2020

M Hand Sanitizer Recalled

On September 9, 2020, Medek, LLC recalled M Hand Sanitizer Alcohol Antiseptic 80% 128 oz/3,785 mL because it may contain methanol, which is toxic when absorbed through the skin or ingested. The product may also have a sub-potent ethanol content, which leads to a lack of efficacy.

Recalls & Warnings

September 10, 2020

Hand Sanitizer Labeled as "Edible" Recalled

On September 3, 2020, CorgioMed LLC recalled one lot of Leafree Instant Hand Sanitizer Aloe Vera because they are labeled "edible alcohol." Hand sanitizers can be toxic if ingested, and can cause lack of coordination, slowed or slurred speech, drowsiness, coma, or death.

Recalls & Warnings

November 24, 2020

Recalled Vitamin D Contains Potentially Dangerous Ingredient

On November 22, 2020, Fusion Health and Vitality LLC recalled all 2020 lots of CORE Essential Nutrients and Immune Boost Sublingual Vitamin D3 because they are adulterated. CORE Essential Nutrients contains the unapproved food additive hordenine HCl.

Recalls & Warnings

November 10, 2020

FDA Warns Immusist for Drug Claims

On October 16, 2020, the FDA issued a warning letter to Immusist, LLC following a review of the company's website, which found statements made about the company's products IMMUSIST Original and IMMUSIST Natural to be drug claims.

Recalls & Warnings

November 10, 2020

Seller of Cholesterol-Lowering Supplements Warned for Drug Claims

On October 29, 2020, the FDA issued a warning letter to Natural Sprout Co.

Recalls & Warnings

October 30, 2020

Seller of Elderberry and Honey Products Warned for COVID-19 Claims

On October 23, 2020, the FDA issued a warning letter to Beepothecary LLC for selling the products BEEHive Delight, BEEbread, and Elderberry, Honey & Propolis Syrup with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

October 30, 2020

Simple Silver Cannot Be Promoted to Prevent or Treat COVID-19

On October 23, 2020, the FDA issued a warning letter to Peterson Research Laboratories LLC for selling the product Simple Silver with unsupported claims that it can treat coronavirus (COVID-19).

Recalls & Warnings

October 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

December 15, 2020

FDA Warns Seller of Evening Primrose Oil and Beta Glucan

On December 2, 2020, the FDA issued a warning letter to Smoky Mountain Naturals, LLC following a review of the company's website, which found statements made about the company's products Evening Primrose Oil and Beta Glucan to be drug claims.

Recalls & Warnings

December 11, 2020

Seller of "Dr. Hotze's Immune Pak" Products Warned for COVID-19 Claims

Seller of "Dr. Hotze's Immune Pak" Products Warned for Coronavirus Claims 

Recalls & Warnings

December 11, 2020

FDA Warns Seller of Curcumin and Cholesterol Supplements

On November 20, 2020, the FDA issued a warning letter to Natures Boost LLC following a review of the company's websites, which found statements made about the company's products Blood Boost Formula and Turmeric Curcumin to be drug claims.

Recalls & Warnings

December 08, 2020

FTC Sends Refund Checks to Consumers of Deceptive Joint Pain Supplement Synovia

On December 1, 2020, the FTC announced it is mailing 13,221 checks totaling nearly $775,000 to consumers who bought Synovia, a supplement intended to treat joint pain and arthritis.

Recalls & Warnings

August 10, 2020

Seller Indicted for Promoting Silver Product as Coronavirus Cure

On July 28, 2020, Utah resident Gordon Pedersen was indicted by a federal grand jury for posing as a medical doctor to sell an unapproved treatment for coronavirus (COVID-19).

Recalls & Warnings

July 28, 2020

Iron Supplements Recalled Due to Undeclared Allergen

Between July 23 and 24, 2020, two companies issued recalls of iron supplements because they may contain undeclared milk.

Recalls & Warnings

July 07, 2020

Sellers of Essential Oils, Hand Sanitizers and More Warned for Coronavirus Claims

The FDA recently issued warning letters to five companies for selling products such as essential oils, homeopathic products, and Chinese herbal products with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

April 10, 2021

Three More Male Enhancement Products Recalled Due to Undeclared Drugs

Between March 30 and April 5, 2021, three companies issued recalls of their male enhancement capsules because FDA analysis found them to contain sildenafil and/or tadalafil.

Recalls & Warnings

December 15, 2020

Mushroom Supplement Seller Warned for Drug Claims

On December 4, 2020, the FDA issued a warning letter to Desert Alchemist LLC following a review of the company's website, social media, and Etsy.com store (www.etsy.

Recalls & Warnings

February 02, 2021

Seller of Aloe Products Warned for Claiming to Treat Joint Stiffness

On January 22, 2021, the FDA issued a warning letter to American Global Health Group, LLC following a review of the company's website, which found statements made about the company's products AloeCure VeraFlex, AloeCure Advanced Formula Capsule, AloeCure Pure Aloe Vera ...

Recalls & Warnings

January 21, 2021

Federal Court Bars Fusion Health From Promoting Vitamin D for COVID-19

On January 8, 2021, the United States Department of Justice announced a permanent injunction has been entered, barring dietary supplement marketer Matthew Ryncarz and his companies Fusion Health and Vitality LLC dba Pharm Origins and Fusion Ionz LLC dba Pharm Origins from making claims that their ...

Recalls & Warnings

January 20, 2021

Seller of Omega-3 Warned for Making Claims to Treat Focus, Mood

On December 9, 2020, the FDA issued a warning letter to Bodyhealth.com, LLC following a review of the company's website, which found statements made about the company's products Healthy-Thin Energize, Body Detox (Oral Spray), and Omega 3 Health to be drug claims.

Recalls & Warnings

December 31, 2020

FDA Warns Seller of Flu Immune

On December 21, 2020, the FDA issued a warning letter to Riverstone LLC for selling the products Flu Immune Drops, L-Lysine, Lysine Extra, and Monolaurin with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

December 31, 2020

FDA Warns Seller of Liposomal Vitamin C, Vitamin D & More

On December 21, 2020, the FDA issued a warning letter to Sparrow Health & Performance LLC for selling the products Organic Liposomal Vitamin C, Nanoemulsified D3K2 (also called Liquid Liposomal Vitamin D3 with K2 or Liposomal Vitamin D3) and Immune Support ...

Recalls & Warnings

March 02, 2021

FDA Warns Seller of Vitamin C, Silver Spray

On March 1, 2021, the FDA issued a warning letter to Ageless Global, LLC following a review of the company's websites for selling Immunoral, Immune Plus, MD Immune Support Spray, and MD CVK-365 Mouth Spray with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

February 22, 2021

FDA Warns Seller of Melatonin & Other Sleep Supplements

On February 18, 2021, the FDA issued a warning letter to SANA Group LLC following a review of the company's website, which found statements made about the company's products Sleep Sana Sleep Drops and Sleep Shots to be drug claims.

Recalls & Warnings

February 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

March 18, 2021

Hand Sanitizer Recalled Because Packaging Resembles Water Bottle

On March 17, 2021, PNHC, LLC d/b/a Heal the World recalled all lots of Heal the World hand sanitizer because the product is packaged in containers resembling water bottles.

Recalls & Warnings

April 02, 2021

Seller of Vision Supplements Warned by FDA

On March 19, 2021, the FDA issued a warning letter to Lipotriad LLC following a review of the company's websites, which found statements made about the company's products Lipotriad Visionary, Lipotriad Adult 50+, Lipotriad Dry Eye, and Lipotriad Vision Support Plus to ...

Recalls & Warnings

May 08, 2021

Seller of Immune Bio Green Cell Warned by FDA

On March 30, 2021, the FDA issued a warning letter to Immune & Genetics Protocols, LLC following a review of the company's websites, which found statements made about the company's product Immune Bio Green Cell to be drug claims.

Recalls & Warnings

June 08, 2021

FDA Warns Seller of "CoronaBox" Containing Vitamin D, Probiotics & More for Unsupported Claims

On May 24, 2021, the FDA issued a warning letter to Everything Health LLC following a review of the company's website by the FDA and Federal Trade Commission (FTC) which found the company promoted its CoronaBox (which contains cordyceps, vitamins, and K2, magnesium, ginger, probiotics ...

Recalls & Warnings

May 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

May 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

January 02, 2012

Manufacturing Violations for Multivitamin, Vitamin K and Other Supplements

On December 19, 2011, the U.S. FDA sent a Warning Letter to Milk Specialties Global regarding manufacturing violations. Affected products include PrimaForce Proliver Capsules, Dr. Mercola Vitamin K2, Active Women’s Multivitamin/Multimineral, Cremagnavol, Immune Support, and HPF Women’s Multi.

Recalls & Warnings

January 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

November 02, 2009

FTC Charges Marketers with Baseless Weight-Loss Claims

On November 2, 2009 the U.S. Justice Department, at the Federal Trade Commission’s request, filed suit today in federal court in a case affecting consumers nationwide.

Recalls & Warnings

February 13, 2016

Cannabis Compound Not Permitted in Supplements, FDA Warns

On February 4, 2016, the FDA issued warning letters to eight companies selling products containing cannabidiol (CBD), a compound derived from cannabis (also known as marijuana). In the U.S., cannabidiol is not permitted to be sold as an ingredient in dietary supplements.

Recalls & Warnings

May 09, 2020

Federal Court Orders Seller to Stop Promoting Silver Product as Coronavirus Cure

On April 29, 2020, a federal court in Utah announced that it has obtained a temporary restraining order preventing Gordon Pedersen and his companies, My Doctor Suggests LLC and GP Silver LLC, from promoting fake treatments for coronavirus (COVID-19).

Recalls & Warnings

May 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

May 02, 2020

Seller of Botanical and CBD Oil Patches Warned for Coronavirus Claims

On April 27, 2020, the FDA issued a warning letter to Santiste Labs LLC for promoting its transdermal patches containing botanical oils and/or CBD with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

March 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

February 18, 2020

Seller of CoQ10, Resveratrol and More Warned for Manufacturing Violations

On February 5, 2020, the FDA issued a warning letter to R-Garden LLC, which found the company's Vitamin O, Gamma-Zyme, L.

Recalls & Warnings

April 11, 2020

FDA Warns Sellers of CBD, Colloidal Silver & Natural Remedies Promoted to Treat Coronavirus

Between April 7 and April 9, 2020, the FDA issued warning letters to five companies for selling products such as CBD, colloidal silver, and natural treatments with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

December 21, 2019

Supplement Company Continues to Make False Claims About Its Products, Says FTC

The FTC has filed a motion of contempt against two supplement companies that, according to the motion, have continued to promote their products with false claims despite being barred from doing so by a previous court order.

Recalls & Warnings

July 06, 2020

FDA Warns Five More Hand Sanitizers May Contain Toxic Ingredient

Update: (7/14/20) The FDA has warned consumers not to use forty-six more hand sanitizers that may contain methanol.

Recalls & Warnings

August 17, 2020

SkinGuard24 Hand Sanitizer Recalled

On August 14, 2020, SG24 LLC recalled SkinGuard24 — All Day Hand Sanitizer because it is labeled as containing methanol, which is toxic when absorbed through the skin or ingested.

Recalls & Warnings

December 01, 2020

Niagen Cannot Be Promoted to Prevent or Treat COVID-19, Warns FDA

On November 17, 2020, the FDA issued warning letters to the sellers of Niagen and Nadovim, supplements that contain different forms of niacin, for selling products with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

October 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.

News Release

May 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.

Recalls & Warnings

November 21, 2024

Douglas Labs Stress-B-Plus Recalled

On October 7, 2024, Nestle Health Science (NHS U.S., LLC) issued a recall of two lots of Douglas Labs Stress-B-Plus because it contains incorrect information on the label.

News Release

April 27, 2004

New ConsumerLab.com report on St. John's wort highlights benefits and risks of herbal product for depression

NEW CONSUMERLAB.COM REPORT ON ST.

Recalls & Warnings

November 26, 2007

Encore Tabs Recalled -- Contain Prescription Drug

On November 21, 2007, Bodee LLC announced today that it is conducting a voluntary nationwide recall of all the company's supplement product sold under the name Encore Tabs.

Recalls & Warnings

April 09, 2006

Sellers of Children’s Weight-Loss Product Settle FTC Charges

On April 6, 2006, the Federal Trade Commission (FTC) announced that the marketers of Pedia Loss, a purported children’s weight-loss product, and Fabulously Feminine, a supposed female libido enhancement product, had agreed to settle Federal Trade Commission charges that they made false and ...

Recalls & Warnings

April 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

September 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

March 14, 2017

Court Shuts Down Supplement Manufacturer

On March 13, 2017, the U.S. District Court for Colorado ordered dietary supplement manufacturers and distributors  EonNutra LLC, CDSM LLC and HABW LLC, and their owner, Michael Floren, to stop all operations until they come into compliance with federal regulations. 

Recalls & Warnings

October 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

June 20, 2020

FTC Warns 30 More Companies for Coronavirus Claims

On June 18, 2020, the FTC announced that it sent warning letters to 30 companies for selling products such as immune system boosters, colloidal silver, vitamin C, and CBD with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

May 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

December 02, 2020

FDA Warns Sellers of Unapproved COVID-19 Tests, CBD Products

On November 23 and November 30, 2020, the FDA issued warning letters to Industry Lab Diagnostic Partners and Avazo-Healthcare, LLC, respectively, for selling unapproved, adulterated, and misbranded tests for coronavirus (COVID-19).

Recalls & Warnings

May 15, 2021

Toxic Hand Sanitizer Recalled

On May 11, 2021 Dibar Nutricional S. de R.L. de C.V. issued a recall of various lots of DIBAR Labs Hand Sanitizer and ProtectoRx Hand Sanitizer because they were confirmed to contain methanol.

Recalls & Warnings

October 09, 2023

Organifi Settles Charges of Unsupported Claims

Organifi, LLC has agreed to pay $150,000 in civil penalties and $50,000 in investigative costs as restitution to settle charges that the company made unsupported claims that its Gold, Pure, Green Juice, and Red Juice products could balance hormone and cortisol levels, regulate the ...

Recalls & Warnings

November 06, 2023

FDA Warns Consumers Not to Use Dr. Ergin’s SugarMD Advanced Glucose Support, Found to Contain Prescription Drugs

On November 3, 2023, the FDA warned consumers not to purchase or use Dr. Ergin’s SugarMD Advanced Glucose Support products after FDA laboratory analysis found the supplement to contain glyburide and metformin.

Recalls & Warnings

November 09, 2023

FDA Warns Biorica International for Cholesterol, Kidney & Cancer Claims

On August 4, 2023, the FDA issued a Warning Letter to Biorica International Corp. following review of the company’s websites and social media, which found statements about the company’s Plaquex Oral Supplements to be drug claims, which are not permitted for dietary supplements.

Recalls & Warnings

April 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.

News Release

April 07, 2004

ConsumerLab.com finds some zinc supplements low in ingredient and many don't instruct on proper use — Consumers urged to learn more about zinc when using supplements

WHITE PLAINS, NY — April 7, 2004 (updated May 4, 2004) — ConsumerLab.com announced today that two of nine zinc pill or liquid supplements that it recently tested contained only 73% to 85% of the claimed amounts.

News Release

March 18, 2004

Many echinacea supplements don't meet quality standards according to ConsumerLab.com — Test results of cold-reducing herbal supplements released

WHITE PLAINS, NY — March 18, 2004 — ConsumerLab.com announced today that five echinacea supplements failed to pass recent independent testing. Lower than claimed amounts of key compounds such as echinacoside and phenols were the most common problem.

News Release

January 09, 2004

USANA products pass ConsumerLab.com screening for substances banned from Olympics

WHITE PLAINS, NY — January 9, 2004 — ConsumerLab.com announced today that six additional products have passed its Athletic Banned Substances Screening Program. ConsumerLab.com tested the products at the request of USANA, a supplement manufacturer. ConsumerLab.

News Release

December 08, 2003

ConsumerLab.com dispels myths about HGH human growth hormone supplements sold widely on Internet

WHITE PLAINS, NY — December 8, 2003 — ConsumerLab.com has released a review of the scientific evidence behind human growth hormone (hGH or HGH) supplements.

News Release

November 02, 2003

Key ingredient missing in some arthritis supplements for people and pets according to ConsumerLab.com — Review of glucosamine, chondroitin and MSM supplements published online today

WHITE PLAINS, NY — November 2, 2003 — ConsumerLab.com today announced test results for supplements used in treating osteoarthritis that contain glucosamine, chondroitin, and/or MSM.

News Release

January 21, 2003

Acidophilus" and other probiotic supplements gain in popularity but live bacteria missing in many — ConsumerLab.com releases review online today

WHITE PLAINS, NY — January 21, 2003 — ConsumerLab.

News Release

December 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

December 10, 2002

Lupus patients cautioned about hormone supplement — ConsumerLab.com releases DHEA testing results online today

WHITE PLAINS, NY — December 10, 2002 — In its latest Product Review, ConsumerLab.com found that 3 of the 17 DHEA (dehydroepiandrosterone) supplement products it tested contained less than their claimed amounts of this hormone — one having less than one-fifth of what it claimed.

News Release

October 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

September 24, 2002

Problems found with most sexual enhancement supplements evaluated by ConsumerLab.com — Only 9 of 22 products pass independent review

WHITE PLAINS, NY — September 24, 2002 — ConsumerLab.com announced today that nearly 60% of products failed to pass its independent Product Review of Sexual Enhancement Supplements. Sexual dysfunction is estimated to affect 43% of women and 31% of men in the U.S.

News Release

August 20, 2002

ConsumerLab.com announces screening of supplements for banned substances for the United States Olympic Committee — First products to pass now listed on ConsumerLab.com web site

WHITE PLAINS, NY — August 20, 2002 — The United States Olympic Committee (USOC) and ConsumerLab.com (CL) announced today that nine products have passed ConsumerLab.com's recently launched Athletic Banned Substances Screening Program. ConsumerLab.

News Release

August 07, 2002

ConsumerLab.com finds some spoilage and inaccuracy among omega-3 and 6 supplements — List released of evening primrose, flaxseed and other GLA/ALA products that passed testing

WHITE PLAINS, NY — August 7, 2002 — ConsumerLab.com, an independent evaluator of health and nutrition products, released results today of its Product Review of Black Currant, Borage, Evening Primrose, and Flaxseed Oils: Sources of ALA and GLA (Omega-3 and -6 Fatty Acids).

News Release

July 10, 2002

Pharmavite dietary supplements receive ConsumerLab.com approval — Vitamin E, SAM-e, St. John's Wort, Ginkgo and others merit approved quality products ranking

WHITE PLAINS, NY — July 10, 2002 — ConsumerLab.

News Release

April 16, 2002

ConsumerLab.com finds "Breast Enhancement" pills lack evidence of efficacy

WHITE PLAINS, NY — April 16, 2002 — ConsumerLab.com announced today that it found no hard evidence to suggest that current dietary supplements marketed for breast enhancement are effective.

News Release

March 28, 2000

Only half of SAM-e supplements found to contain proper ingredients and labeling in ConsumerLab.com testing; Product Review of popular anti-depressant published online today.

WHITE PLAINS, NY, March 28, 2000 — Among 13 brands of SAM-e dietary supplements (used primarily in treating depression and osteoarthritis) only seven were found to contain labeled amounts of SAM-e (S-adenosyl-methionine). These results were reported today by ConsumerLab.

News Release

March 07, 2000

ConsumerLab.com finds many arthritis supplements lacking labeled ingredients; Glucosamine and Chondroitin product review published online today.

WHITE PLAINS, NY, March 7, 2000 — Among 25 major brands of supplements containing glucosamine and/or chondroitin used for treating osteoarthritis, nearly one-third were found not to contain all labeled ingredients. These results were reported today by ConsumerLab.

News Release

August 05, 1999

ConsumerLab.com initiates independent testing of herbal products and supplements. Certification Seal announced.

WHITE PLAINS, NY, August 5, 1999 — ConsumerLab.com, LLC announced that it has begun a large-scale program of independent testing of herbal products and dietary supplements. .

Recalls & Warnings

June 20, 2017

Beware of Bodybuilding Supplements, FDA Warns

On June 20, 2017, the FDA warned consumers to beware of bodybuilding products because a number of these products have been found to contain steroids or steroid-like substances. Such products could cause serious and even life-threatening health risks, including: 

Recalls & Warnings

December 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

April 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

December 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

January 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

January 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

April 27, 2023

FTC Returns over $1.1 Million to Consumers for RevMountain Teeth Whitening Products

On April 25, 2023, the FTC announced it will be returning over $1.

Recalls & Warnings

May 01, 2023

TruVision Recalls Products Due to Presence of Potentially Dangerous Ingredients

On April 27, 2023, TruVision Health issued a recall of various dietary supplement products because they contain hordenine and/or octodrine/DMHA, compounds that the FDA considers to be “possibly unsafe” and which are not permitted to be sold as dietary supplements.

Recalls & Warnings

July 06, 2022

FDA Warns Kratom Companies for Arthritis, Pain Relief Claims & More

On January 30, 2022, the FDA issued warning letters to four sellers of kratom products because they were promoted to treat pain relief, opioid withdrawal, blood sugar control, anxiety, and to treat rheumatoid arthritis.

Recalls & Warnings

June 16, 2004

FTC Challenges Ads for Kids’ Weight Loss Pill and Female Sexuality Supplement

On June 16, 2004 The Federal Trade Commission announced that it had charged three Florida-based companies and their principals with making false and unsubstantiated claims in connection with the advertising for “Pedia Loss,” a purported children’s weight loss product.

Recalls & Warnings

December 06, 2011

FTC Stops Operator of Fake News Sites Offering Acai and Colon Cleanse Products

On December 1, 2011, The Federal Trade Commission announced that it has filed a complaint jointly with the State of Connecticut, seeking to permanently stop a Connecticut-based operation that allegedly used fake news websites to promote their products, made deceptive weight-loss claims, and told ...

Recalls & Warnings

April 09, 2019

Dangerous Levels of Lead and Nickel Found in Kratom Products

On April 3, 2019, the FDA released the results of its tests that found dangerous levels of lead and nickel in certain kratom products. The agency tested 30 products sold on websites such as krakenkratom.com and by retailers such as Gaia Ethnobotanicals, Sunstone Organics LLC and Happy Hippo LLC.

Recalls & Warnings

April 03, 2020

FDA Warns Seller of FullerLifeC60 for Coronavirus Claims

On March 30, 2020, the FDA issued a warning letter to FullerLifeC60, LLC, for selling a product with unsupported claims that it can treat coronavirus (COVID-19).

Recalls & Warnings

February 01, 2022

Complaint Submitted to FTC for doTerra Essential Oil COVID Claims

On January 28, 2022, the website truthinadvertising.org submitted a complaint to the Federal Trade Commission (FTC) against doTerra International, LLC. following a series of Zoom calls from the company titled "Protocols for the Current Climate.

Recalls & Warnings

June 17, 2022

Built Brand Protein Bar Recalled Due to E. Coli Concern

On June 10, 2022, Built Brands, LLC. Issued a recall of 4,146 Banana Cream Pie Puffs protein bars after routine testing discovered potential contamination with E. coli (Escherichia coli).

Recalls & Warnings

February 06, 2023

FDA Warns Companies Promoting Products to Treat Monkeypox, COVID-19, & Other Viruses

On January 30, 2023, the FDA issued a warning letter to four companies following review of the company websites, which found statements about company products to be drug claims because they were promoted to mitigate, prevent, treat, diagnose, or cure viruses such as monkeypox.

Recalls & Warnings

July 19, 2011

Recall of Enhancement Supplement for Men - Contains Drug Compounds

On July 13, 2011, Global Wellness, LLC announced an expanded voluntary nationwide recall of Via Extreme Ultimate Sexual Enhancer Dietary Supplement for Men. The product was distributed throughout the U.S. Puerto Rico, Barbados, and Canada to internet and retail consumers.

Recalls & Warnings

January 13, 2015

Seller of Speech Disorder Supplement Agrees to Settle FTC Charges of Deceptive Claims

NourishLife, LLC, seller of supplements promoted for treating children's speech disorders, has agreed to pay $200,000 in order to settle FTC charges that claims made on the company's website and in brochures were deceptive and not supported by science.

Recalls & Warnings

May 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

April 29, 2013

Recall: Multivitamin Containing Undeclared Milk

On April 26, 2013, Saratoga Therapeutics, LLC issued a recall of ebA Multivitamin Supplement because it may contain undeclared milk. The label describes the supplement as free of milk components.

Recalls & Warnings

February 20, 2013

Recall: Arthritis and Muscle Pain Supplement Contains Prescription Drugs

On February 15, 2013, Reumofan Plus USA, LLC and Reumofan USA, LLC announced a recall of Reumofan Plus, a dietary supplement promoted for arthritis and muscle pain, because it was found to contain the active pharmaceutical ingredients methocarbamol, dexamethasone, and diclofenac.

Recalls & Warnings

January 18, 2013

FTC Upholds Ruling, POM Wonderful Health Claims Were Deceptive

On January 16, 2013, the Federal Trade Commission (FTC) announced it will uphold a judge’s ruling that makers of POM Wonderful 100% Pomegranate Juice and POMx supplements made deceptive and unsubstantiated claims that the products could treat, prevent, or reduce the risk of heart disease, prostate ...

Recalls & Warnings

April 28, 2017

Marketers of Weight Loss System Agree to Settle FTC Charges of Deceptive Claims

On April 21, 2017, the FTC announced the marketers of the NutriMost Ultimate Fat Loss System (NutriMost, LLC and NutriMost Doctors, LLC) agreed to settle charges they made false claims about the product.

Recalls & Warnings

January 12, 2016

Twenty-four Male Enhancement Supplements Recalled

On January 9, 2016, R Thomas Marketing LLC. in conjuction with Just Enhance LLC, issued a recall of the following sexual enhancement supplements because they were found to contain sildenafil:

Recalls & Warnings

October 11, 2016

Seller of Glucosamine and Chondroitin Settles FTC Charges of False Advertising

On October 5, 2016, the FTC announced the sellers of the liquid glucosamine and chondroitin supplement Supple (Supple LLC) agreed to settle charges they made false claims about the product.

Recalls & Warnings

September 06, 2016

Seller on Noni Juice Warned for Manufacturing Violations, Drug Claims

On August 26, 2016, the FDA issued a warning letter to Healing Noni Co. L.L.C.

Recalls & Warnings

January 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

December 08, 2011

HCG Diet Products Don't Work and Are Illegal Says FDA

On December 6, 2011, the U.S. FDA warned consumers to avoid homeopathic HCG weight-loss diet products because they don't work, often make unsupported claims, and are illegal for sale. In addition, some of these products direct user to follow a potentially dangerous diet.

Recalls & Warnings

May 24, 2021

U.S. Marshals Seize $1.3 Million Worth of Kratom

U.S. Marshals have seized approximately $1.3 million worth of bulk kratom and kratom supplements manufactured by Atofil, LLC, a subsidiary of Premier Manufacturing Products, according to the FDA.

Recalls & Warnings

September 24, 2020

FTC Sends Refund Checks to Consumers of Deceptive Joint Pain Supplement

On September 24, 2020, the FTC announced it is mailing 4,782 checks totaling more than $76,000 to consumers who bought Isoprex, a supplement marketed with deceptive claims that it could treat or cure joint pain, muscle pain, headaches, and arthritis.

Recalls & Warnings

August 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

August 25, 2020

Seller of CBD and NAC Warned for Coronavirus Claims

On August 19, 2020, the FDA issued a warning letter to Living Senior, LLC for selling CBD and NAC products with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

August 18, 2020

Seller of Immune Shot Criminally Charged With Making Coronavirus Claims

On August 10, 2020, prosecutors in Georgia charged Matthew Ryncarz and his company Fusion Health and Vitality, LLC d/b/a/ Pharm Origins with selling the misbranded product Immune Shot.

Recalls & Warnings

July 29, 2020

Herbacil Antiseptic Hand Sanitizer Recalled

On July 27, 2020, Broncolin S.A. de C.V. recalled Herbacil Antiseptic Hand Sanitizer 70% Alcohol because it may contain methanol, which is toxic when absorbed through the skin or ingested.

Recalls & Warnings

July 10, 2020

Seller of Hand Sanitizer "Alternative" Warned for Coronavirus Claims

On July 7, 2020, the FDA issued a warning letter to Ionogen, LLC for selling products with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

March 04, 2022

FTC, FDA, and DOJ Take Joint Action Against Herbal Tea Companies for COVID Claims

On March 3, 2022, the FDA, FTC, and DOJ sued a New York-based marketer of herbal tea, in attempts to permanently block deceptive ads that claim Earth Tea is clinically proven to treat, cure, and prevent COVID-19.

Recalls & Warnings

June 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

December 07, 2011

Maker of PowerGum and Colon Cleanser Warned of Violations by FDA

The U.S. FDA published a Warning Letter (dated 12/1/11) to DreamLife, LLC regarding violations of Current Good Manufacturing Practices at its manufacturing facility in Louisana and labeling violations on its PowerGum and Extreme Colon Cleanser products.

Recalls & Warnings

October 05, 2011

FDA Warns Nature's Rite of Promoting 8 Supplements as Drugs

The FDA published a Warning Letter dated September 19, 2011 to Nature's Rite, LLC stating that the firm’s online promotion of its various supplements for the treatment or prevention of various diseases cause these products to be considered unapproved drugs.

Recalls & Warnings

June 21, 2005

FTC Settles Claims with Marketers of FiberThin and Propolene

On June 20, 2005, the Federal Trade Commission (FTC) announced that the marketers of the dietary supplements FiberThin and Propolene have settled FTC charges that their misleading weight-loss claims violated federal laws.

Recalls & Warnings

July 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

November 21, 2012

Maker of Probiotic and Sports Drinks Warned For Manufacturing Violations

On November 6, 2012, the FDA issued a warning letter to CocoKefir, LLC stating that the company's Tula's CocoKefir, Tula's Citrus CocoKefir, and Tula's Apple Cinnamon CocoKefir have been prepared, packed or held under conditions which violate Current Good Manufacturing Practices.

Recalls & Warnings

June 07, 2013

Seller of Red Rice Yeast With CoQ10, Respiratory Supplement And More Warned For Manufacturing Violations and Drug Claims

On February 25, 2013, the FDA issued a warning letter to Altasource, LLC, dba Meta Labs LLC, following a facility inspection which found the company's dietary supplements, including Respiratory Response, African Mango, Coffee Black Salve, Meta-Cell, Conjugated Linoleic Acid and Red Yeast Rice with ...

Recalls & Warnings

August 07, 2018

FDA Warns Seller of Noni Juice Products

On July 18, 2018, the FDA issued a warning letter to Hawaiian Organic Noni, LLC, following a facility inspection which found statements made on the labels of certain products, including Hawaiian Organic Noni Fruit Leather, Hawaiian Organic Noni Banana Fruit Leather, Hawaiian Organic Noni ...

Recalls & Warnings

June 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

June 16, 2020

NutraCap Labs Warned for Unsafe Ingredients and Manufacturing Violations

On May 21, 2020, the FDA issued a warning letter to NutraCap Labs LLC, which found the company's products to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for dietary supplements.

Recalls & Warnings

June 16, 2020

Seller of Silver, Arginine, and More Warned for Manufacturing Violations

On June 1, 2020, the FDA issued a warning letter to Morningstar Minerals LLC, which found the company's products, including Silver Boost, to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for dietary ...

Recalls & Warnings

June 23, 2020

KBMO Diagnostics Warned for Unapproved COVID-19 Test

On June 17, the FDA issued a warning letter to KBMO Diagnostics, LLC for selling the product COVID-19 Fingerstick Test Kit, an unapproved, adulterated and misbranded antibody test for coronavirus (COVID-19).

Recalls & Warnings

May 23, 2020

BIOTA Biosciences Recalls Injectable CBD and Curcumin Products

On May 20, 2020, BIOTA Biosciences LLC issued a recall of five lots of three injectable products because they were marketed without FDA approval.

Recalls & Warnings

May 28, 2020

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

On May 26, 2020, the FDA issued warning letters to four companies for selling products such as CBD, essential oils, colloidal silver, and vitamins with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

May 26, 2020

Seller of Vitamin and CBD "NoronaPak" Warned for Coronavirus Claims

On May 21, 2020, the FDA issued a warning letter to Apollo Holding LLC for promoting a kit containing vitamins and CBD with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

June 05, 2020

Seller of Silver and Vitamin C Lozenges & More Warned for Coronavirus Claims

On June 1, 2020, the FDA issued a warning letter to Dr.

Recalls & Warnings

June 05, 2020

Seller of CBD, Sleep Aids, and Cold & Flu Products Warned for Manufacturing Violations

On April 28, 2020, the FDA issued a warning letter to The Dragontree Apothecary LLC, which found the company's Sleep Support, Anxiety Relief, Cold & Flu Relief, and Inflammation Relief to be adulterated because they were prepared, packed, or held under conditions that ...

Recalls & Warnings

April 25, 2020

Injectable Curcumin, CBD Are Not Safe, Warns FDA

On April 9, 2020, the FDA issued a warning letter to BIOTA Biosciences LLC following a review of the company's website, which found statements made about some of the company's, products, including Canabidiol (CBD) Complex, Cannabidiol+Curcumin, and Curcumin Complex to be ...

Recalls & Warnings

April 17, 2020

Seller of Vitamin D, MSM, Selenium & More Warned for Drug Claims

On March 31, 2020, the FDA issued a warning letter to KetoKerri LLC following a review of the company's website, which found statements made about some of the company's products, including Dr.

Recalls & Warnings

May 12, 2020

FDA Warns Seller of "COVID-19 Cough Syrup"

On May 8, 2020, the FDA issued a warning letter to Seanjari Preeti Womb Healing, L.L.C. for selling its product COVID-19 Cough Syrup with unsupported claims that it can treat coronavirus (COVID-19).

Recalls & Warnings

December 05, 2019

Joint Supplement Synovia Was Promoted With Phony Testimonials, Says FTC

A.S. Research, LLC, has agreed to settle Federal Trade Commission (FTC) charges that they deceived consumers with false claims that their dietary supplement Synovia could treat arthritis and alleviate joint pain.

Recalls & Warnings

April 03, 2020

Gaia's Whole Healing Essentials Warned for Colloidal Silver Coronavirus Claims

On April 1, 2020, the FDA issued a warning letter to Gaia's Whole Healing Essentials, LLC, for selling products with unsupported claims that they can treat coronavirus (COVID-19).

Recalls & Warnings

November 02, 2019

Brain Supplement Claims to Treat Brain Injuries, Alzheimer's Are Deceptive, Says FTC

On November 1, 2019 the FTC filed a lawsuit against Neora LLC (formerly Nerium International) for making false claims that the supplement Neora EHT (formerly called Nerium EHT) can treat concussions and chronic traumatic encephalopathy caused by repetitive brain trauma, Alzheimer's ...

Recalls & Warnings

October 22, 2019

Company Marketing CBD for Use in Infants and Children Gets Strong Warning

On October 10, 2019, the FDA and FTC issued a joint warning letter to Rooted Apothecary LLC for "illegally selling unapproved products containing cannabidiol (CBD) online with unsubstantiated claims" including that the products could treat teething pain and ear aches in infants, autism, ...

Recalls & Warnings

October 22, 2019

Seller of TrueAloe and AloeCran Settles Charges of Making False Claims

NatureCity, LLC, has agreed to settle Federal Trade Commission (FTC) charges that they deceived consumers by making false claims about their TrueAloe and AloeCran products.

Recalls & Warnings

July 12, 2019

PROBAR Meal Bars Recalled

On July 11, 2019, PROBAR LLC issued a recall of certain flavors and lots of its Meal® bars because they may contain undeclared milk and soy allergens. There has been one report of an allergic reaction to-date.

Recalls & Warnings

February 04, 2020

Seller of Digestion Supplements Warned for Manufacturing Violations

On January 10, 2020, the FDA issued a warning letter to Marco Pharma International LLC, which found the company's  Absinthium Herbal Liquid Extract 100 ml (Absinthium), promoted for "digestive support", and other products, including S21 Multi Somaplex 100 ml (Multi Somaplex), ...

Recalls & Warnings

January 28, 2020

Weight Supplement Contains Hidden Drug

On January 13, 2020, the FDA issued a warning letter to Wave Miami, LLC because the company's weight loss supplement, Lipro Dietary Capsule was found to contain the prescription medication tadalafil.

Recalls & Warnings

April 14, 2020

Teami Tea Settles Charges of Unproven Claims and Deceptive Celebrity Endorsements

On March 6, 2020, the FTC announced that Teami, LLC, a marketer of tea and skin care products, agreed to settle charges that it was selling products with unproven claims and misleading celebrity endorsements.

Recalls & Warnings

April 17, 2020

Arthritis Supplement Recalled for Salmonella Risk

On April 13, 2020, Arthri-D, LLC issued a recall of one lot of Arthri-D arthritis supplement because recent testing found it has the potential to be contaminated with Salmonella.

Recalls & Warnings

April 20, 2021

Chiropractor Who Claimed Vitamin D and Zinc Work Better Than COVID Vaccines Charged by FTC

On April 15, 2021, the FTC charged St.

Recalls & Warnings

February 09, 2021

Three More Hand Sanitizers Contain Toxic Ingredient

Between February 3 and 5, 2021, the FDA issued warning letters to three sellers of hand sanitizers because laboratory tests showed that their products contain methanol, which is toxic when absorbed through the skin or ingested.

Recalls & Warnings

November 01, 2017

Hemp Oil and Cannabidiol (CBD) Marketers Warned by FDA Over Claims

On November 1, 2017, the FDA announced it issued warning letters to four companies promoting products containing cannabidiol (CBD), a compound derived from cannabis (also known as marijuana), for the treatment of cancer, as well as other diseases, such as Alzheimer's disease. In the U.

Recalls & Warnings

November 07, 2005

FTC Stops Bogus Ads for "Bio Trim" and Other Weight-loss Products

On November 7, 2005, the Federal Trade Commission (FTC) announced that under the terms of a consent agreement that it has approved, Tustin, California based Natural Products, LLC, All Natural 4 U, LLC and their owner, Ana M.

Recalls & Warnings

June 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

November 01, 2017

FDA Warns Sellers of Bodybuilding Supplements Containing Steroid-Like Substances

On October 23, 2017, the FDA issued warning letters to three supplement distributors because several of their bodybuilding products contain selective androgen receptor modulators (SARMs).

Recalls & Warnings

August 03, 2017

AMPT "Sexual Enhancement" Coffee Recalled

On August 1, 2017, AMPT Life, LLC, recalled all lots of AMPT Coffee after FDA testing found sildenafil and tadalafil. 

Recalls & Warnings

July 18, 2017

Herbal "Sexual Enhancement Coffee" Recalled

On July 13, 2017, Bestherbs Coffee LLC recalled their product New Kopi Jantan Tradisional Natural Herbs Coffee after FDA testing found desmethyl cabodenafil.

Recalls & Warnings

September 08, 2017

Probiotic for Infants Recalled Due to Potential Choking Hazard

On September 7, 2017, Garden of Life, LLC, issued a recall of Baby Organic Liquid, a liquid probiotic supplement for infants, because the product, as labeled, includes directions for use that may be misinterpreted and could pose a choking hazard due to the thickness of the liquid.

Recalls & Warnings

October 29, 2016

Steroid "Alternatives" Not Permitted In Dietary Supplements, FDA Warns

On September 27, 2016, the FDA issued a warning letter to Proprietary Wellness, L.L.C.

Recalls & Warnings

July 23, 2016

Seller of GlucoCor Warned for Drug Claims

On June 30, 2016, the FDA issued a warning letter to MC-COR, LLC, following a review of the company's website and Facebook page which found statements made about its GlucoCor capsules to be drug claims.

Recalls & Warnings

August 05, 2016

Seller of Fertilix Warned By FDA

On July 22, 2016, the FDA issued a warning letter to CellOxess LLC, following a review of the company's websites, social media pages and marketing literature which found statements made about Fertilix Preconceptual, Fertilix Low Dose and Fertilix Max to be drug claims.

Recalls & Warnings

May 17, 2016

Sexual Enhancement Supplement Contains Undeclared Drugs

On May 6, 2016, the FDA issued a warning letter to Economax, LLC because the company's sexual enhancement supplement, Super Power Khan was found to contain sildenafil and hydroxyhomosildenafil.

Recalls & Warnings

May 02, 2016

Liquid Multi Recalled Due to Allergen Risk

On April 26, 2016, Schaffner Distributing Pronutri LLC. issued a recall of Re-VITA-lize Whole Food Liquid Vitamin (in tropical orange flavor) because it contains undeclared soy lecithin. 

Recalls & Warnings

November 21, 2015

FTC Charges Maker of Supplement for Opiate Addiction with Deceptive Claims

On November 16, 2015, the FTC filed a lawsuit against Sunrise Nutraceuticals, LLC, charging that the company made deceptive claims its product, Elimidrol, can alleviate opiate withdrawal symptoms and increase a user's likelihood of overcoming opiate addiction. 

Recalls & Warnings

September 02, 2015

Antioxidant Supplement Recalled

On August 28, 2015, VRVK Nutraceuticals, LLC, DBA Dr. Venessa's Formulas, issued a voluntary recall of Ultimate Antioxidant Tablets because they may contain the undeclared allergens crustacean shellfish and milk.

Recalls & Warnings

April 17, 2018

Sexual Enhancement Supplement Recalled

On April 16, 2018, Epic Products, LLC, recalled its sexual enhancement supplement Euphoric because it was found to contain undeclared sildenafil and tadalafil.

Recalls & Warnings

August 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

October 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

October 06, 2006

FDA Warns Mangosteen Juice Maker of Drug Promotions

On September 20, 2006, the U.S. Food and Drug Administration (FDA) sent a Warning Letter to the makers of Xango, a mangosteen juice product. The letter advised that distributors of the product were using brochures making health claims restricted to the promotion of drugs.

Recalls & Warnings

September 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

November 21, 2012

Distributor Warns of Counterfeit Liquid Energy Shots

On November 19, 2012, Living Essentials LLC announced the company discovered and halted the production of counterfeit versions of 5-hour ENERGY® liquid energy shots. The company filed suits against the counterfeiters in U.S.

Recalls & Warnings

January 04, 2012

Seller of "HCG Drops" for Weight Loss Warned by FDA and FTC of Violations

On December 21, 2011, the U.S. FDA and FTC sent a joint Warning Letter to hCG Drops LLC regarding its marketing of Slim Diet Drops. According to the letter, the product is considered an unapproved drug because it is promoted for drug-like uses on the company's website, including the following:

Recalls & Warnings

June 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

May 24, 2013

Brewable Tea and Tea Supplement Company Warned For Manufacturing Violations and Drug Claims

On April 2, 2013, the FDA issued a warning letter to Natures Health Options, LLC, following an investigation which found the company's Charantea Bitter Melon Ampalaya, which is distributed as a dietary supplement in capsule form, and as a tea, to be adulterated because it was prepared, packed, or ...

Recalls & Warnings

May 24, 2013

Maker of Neuropathic Pain Product Warned For Drug Claims, Misbranding

On April 11, 2013, the FDA issued a warning letter to Realm Labs, LLC, following a review of the company’s websites which found statements made about its NeuRemedy products to be drug claims.

Recalls & Warnings

August 28, 2013

Tea and Papaya Supplement Company Warned For Drug Claims

On August 12, 2013, the FDA issued a warning letter to Herbal Papaya, LLC, following a review of the company's website and Facebook page which found statements made about Papaya Seed Extract Capsules, 100% Papaya Leaf (Paw Paw Twig) and Papaya Leaf with Rooibos Tea to be drug claims. 

Recalls & Warnings

August 08, 2013

Sleep Supplement Recalled Due To Undeclared Drugs

On August 7, 2013, Health and Beyond LLC issued a voluntary recall of dietary supplement Tranquility because it was found to contain traces of undeclared drugs, Doxepin and Chlorpromazine.

Recalls & Warnings

August 06, 2013

Maker of Greens and Whole Foods Supplements Warned For Drug Claims, Manufacturing Violations

On July 19, 2013, the FDA issued a warning to ProNatural Nutrition, LLC, following a facility inspection which found that statements made on product labels, including "Healing to cells and tissues," and "Non-toxic antibiotic" to be drug claims.

Recalls & Warnings

November 14, 2012

Maker of Vitamin C, Aloe and Sexual Enhancement Supplements Warned for Drug Claims and Misbranding

On October 22, 2012, the FDA issued a warning letter to Health Breakthroughs International, LLC after a review of the company's product labels and website found the dietary supplements Amazing C, MPS-Gold 100 and Power Herbal Formula to be promoted as drugs.

Recalls & Warnings

July 24, 2012

Baby Supplement Recalled Due To Salmonella Risk

On July 20, 2012, Wellements LLC issued a voluntary recall of Baby Move Prune Concentrate because testing of retained raw materials used in the product found one ingredient to be positive for Salmonella.

Recalls & Warnings

June 13, 2012

Lack of Quality Control and Unapproved Claims by Supplement Seller

On May 14, 2012, the U.S. FDA sent a Warning Letter to Caribe Natural, LLC, distributor of GERMA brand dietary supplements, regarding violation of various FDA requirements.

Recalls & Warnings

May 16, 2012

Reaction Nutrition Warned by FDA of Violations in Manufacturing and Promotion of Several Supplements

On May 8, 2012, the U.S. FDA warned Reaction Nutrition, L.L.C. of Carnegie, PA of violations of Current Good Manufacturing Practices for dietary supplements and of illegally promoting a supplement as a drug.

Recalls & Warnings

May 07, 2012

FDA Warns Doctor Promoting Own Supplements Online as Treatments

On April 18, 2012 the U.S. Food and Drug Administration (FDA) sent a Warning Letter to Jacob Teitelbaum, M.D. of Fatigued to Fantastic, LLC regarding the promotion that company's products on its website www.endfatigue.com.

Recalls & Warnings

February 13, 2013

Herbal Supplement Maker Warned For Manufacturing Violations, Misbranding

On February 6, 2013, the FDA issued a warning letter to Genesis Herb Company LLC, following a facility inspection which found the company's Seizure, Relax, Formula ARTH, Disintegrate, Gout, Plantain, and Colloidal Silver dietary supplements to be adulterated because they were prepared, packed, or ...

Recalls & Warnings

September 16, 2015

Herbal Extracts Recalled

On September 15, 2015, Iowa Select Herbs, LLC issued a recall of numerous herbal exacts following a permanent injunction which required the company to stop selling supplements.

Recalls & Warnings

December 19, 2013

Maker of Joint Health Supplements Warned for Manufacturing Violations

On December 4, 2013, the FDA issued a warning letter to PurQuality, LLC.

Recalls & Warnings

August 03, 2018

Vanilla Almond Breeze Almond Milk Recalled

On August 2, 2018, HP Hood LLC issued a recall of half-gallon (1.89 L) cartons of refridgerated Vanilla Almond Breeze almond milk because the product may contain milk, an allergen not listed on the label.

Recalls & Warnings

July 18, 2018

Maker of Vitamin B12 and Multimineral Supplements Warned by FDA

On July 6, 2018, the FDA issued a warning letter to Aegle Nutrition, LLC, following a facility inspection which found some of the company's products, including Tropical Oasis Ionized Trace Minerals, Tropical Oasis Ultra Methyl B12, and Tropical Oasis Premium Vitamin B12 to be ...

Recalls & Warnings

May 07, 2019

"The Beast" Supplement for Men Recalled

On May 7, 2019, STIFF BOY LLC issued a recall of The Beast, a supplement promoted for male sexual enhancement, because FDA analysis found it to contain sildenafil.

Recalls & Warnings

April 12, 2019

Sexual Enhancement Supplement for Men Recalled

On April 9, 2019, SD Import, LLC issued a recall of Aphrodisiac, a supplement promoted for male sexual enhancement, because FDA analysis found it to contain sildenafil.

Recalls & Warnings

February 09, 2019

Herbal Skin Remedy Recalled, Can Cause Serious Injury

On February 8, 2019, McDaniel Life-Line LLC issued a recall of all lots of Indian Herb a product marketed to be taken orally or applied topically, as a remedy for abnormal skin growths.

Recalls & Warnings

November 24, 2018

Dangerous Drug In Supplements for Pain and Anxiety

On November 20, 2018, the FDA announced it has issued warning letters to two companies for the illegal marketing of products labeled as dietary supplements that contain the opioid-like drug tianeptine.

Recalls & Warnings

September 19, 2018

FDA Warns Seller of Shilajit

On September 6, 2018, the FDA issued a warning letter to Adaptive Energy LLC, following an inspection of the company's website, which found statements made about its shilajit product, Purblack were found to be drug claims.

Recalls & Warnings

March 23, 2019

DG Health NATURALS Baby Cough Syrup Recalled

On March 20, 2019, Kingston Pharma, LLC issued a recall of all lots of DG/health NATURALS baby Cough Syrup + Mucus because it has the potential to be contaminated with Bacillus cereus/Bacillus circulans.

Recalls & Warnings

February 19, 2019

DG Baby Gripe Water Herbal Supplement Recalled

On February 15, 2019, Kingston Pharma, LLC issued a recall of all lots of DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts due to the presence of an undissolved ingredient, citrus flavonoid.

Recalls & Warnings

June 25, 2019

Kratom Is Dangerous and Not Proven to Treat Addiction, FDA Warns Marketers

On June 25, 2019, the FDA issued warning letter to two marketers and distributors of kratom products, listed below, for illegally selling unapproved, misbranded kratom-containing drug products with unproven claims about their ability to treat or cure opioid addiction and withdrawal symptoms.

Recalls & Warnings

August 16, 2018

Kratom Recalled Due to Salmonella Risk

On August 14, 2018, Zakah Life, LLC issued a recall of Super Green Maeng Da Premium Kratom powder, Powerful Red Vein Bali Premium Kratom powder, Super Green Maeng Da Premium Kratom capsules, and Powerful Red Vein Bali Premium Kratom capsules because laboratory testing revealed the presence of ...

Recalls & Warnings

May 29, 2018

FDA Warns Seller of "Aromatase Inhibitor" Supplement

On May 18, 2018, the FDA issued a warning letter to Performance Nutrition Formulators LLC d.b.a. VMI Sports because its product Arimistane contains Androsta-3,5-Diene-7,17-Dione, an ingredient that the FDA considers to be a new drug and not a dietary supplement ingredient.

Recalls & Warnings

May 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

April 21, 2018

Triangle Pharmanaturals Expands Recall of Kratom Products

On April 17, 2018, Triangle Pharmanaturals, LLC, expanded its original recall of kratom-containing products to include 26 additional kratom products.

Recalls & Warnings

April 21, 2018

NutriZone Expands Recall of Kratom Products

On April 18, 2018 NutriZone LLC expanded its original recall of kratom-containing products to include 29 additional kratom products.

Recalls & Warnings

April 17, 2018

Seller of Osha and Cayenne Supplements & More Warned for Manufacturing Violations

On March 21, 2018, the FDA issued a warning letter to Secret Garden of Health & Healing, LLC, following a facility inspection which found a number of the company's products, including Osha Root and Cayenne, to be adulterated because they were prepared, packed, or held under conditions that ...

Recalls & Warnings

January 21, 2018

Joint Supplement Recalled for Salmonella Risk

On January 21, 2018, Arthri-D, LLC announced a recall of its joint pain supplement, Arthri-D (120 count), due to possible Salmonella contamination.

Recalls & Warnings

January 19, 2018

Flawless Beauty Shut Down, Company's Kits and Products Recalled

On January 19, 2018, Flawless Beauty, LLC issued a recall for all lots of nineteen products sold individually or together as part of its "whitening kits."  

Recalls & Warnings

January 16, 2018

Marketers of CellAssure and Cognify Settle FTC Charges of Deceptive Cancer Claims

On January 11, 2018, the FTC announced that CellMark Biopharma, LLC and its CEO, Derek E.

Recalls & Warnings

January 13, 2018

Seller of Depression, Prostate Supplements & More Warned for Manufacturing Violations, Drug Claims

On August 21, 2017, the FDA issued a warning letter to Irmo-Vita, LLC, following a facility inspection which found that several of the company's products, including Hysta-Min, Man-Affirm, Phung-EX, and Bacto- EX to be adulterated because they were prepared, packed, or held ...

Recalls & Warnings

December 26, 2017

Seller of BrainAlert Warned for Manufacturing Violations, Drug Claims

On December 14, 2017, the FDA issued a warning letter to BrainAlert, LLC.

Recalls & Warnings

March 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

March 06, 2018

Protein Bars Recalled Due to Undeclared Allergens

On March 5, 2018, IDLife, LLC, issued a recall of their Protein Bars, Snack Bars, and Kids Bars because they may contain undeclared almonds, peanuts, and/or coconut oil.

Recalls & Warnings

February 10, 2018

Warning to D-Limonene, Vitamin C Seller

On January 31, 2018 the FDA issued a warning letter to Long Life Unlimited, LLC following a review of the company's website which found promotional statements and testimonials made about products including Balance 600, D-Limonene, Rapha Remedy, Rapha Remedy w/ p73 Wild Oregano, Vitamin C, ...

Recalls & Warnings

February 02, 2018

Seller of Vitamin D, Omega-3's, Whey Protein & More Warned for Drug Claims

On January 24, 2018 the FDA issued a warning letter to Young Health Products, LLC following a review of the company's website which found promotional statements and testimonials made about the certain products, including Lugol's Solution 2%, Liquid Vitamin D3, Probimune, Flax Seed & Omega ...

Recalls & Warnings

August 23, 2015

Maker of Herbal Supplements Sold on eBay, Amazon and Other Websites Shut Down

On August 17, 2015, a federal court ordered a permanent injunction against dietary supplement company Iowa Select Herbs LLC for unlawfully manufacturing and distributing unapproved new drugs and misbranded drugs and adulterated and misbranded dietary supplements.

Recalls & Warnings

November 10, 2015

"Natureal" Weight Supplement Recalled

On November 9, 2015 Inaffit, LLC issued a voluntary recall of all lots of weight loss supplement Natureal because it was found to contain undeclared sibutramine.

Recalls & Warnings

April 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

March 17, 2015

Seller of Tea Warned for Drug Claims

On March 4, 2015, the FDA issued a warning letter to Four Elements Organic Herbals, LLC because statements made about HERBAL TEA Power, Energy & Stamina, ORGANIC HERBAL TEA Tulsi TelepaTea, ORGANIC HERBAL TEA To Your Health, Hawthorn Fresh Herb Extract, Elderberry Fresh Herb ...

Recalls & Warnings

February 28, 2015

Drugs Found in Male Enhancement Supplements

On December 11, 2014, the FDA issued a warning letter to Biogenix USA, LLC, following a facility inspection which found the company's sexual enhancement products, HAM, CE6 and SARMZ to contain undeclared drugs, as well as drugs which were listed on the label but are not permitted ...

Recalls & Warnings

February 17, 2015

Seller of Muscle Supplements Containing Synthetic Steroids Warned

On February 9, 2015, the FDA issued a warning letter to A2Z Industries, LLC, following a facility inspection which found the company's muscle enhancing supplements, including HaloV and EPI2A3A to be labeled as containing synthetic steroids.

Recalls & Warnings

February 06, 2015

Seller of Aloe Supplement Warned for Drug Claims

On January 21, 2015, the FDA issued a warning letter to Pristine Nutraceuticals, LLC, following a review of the company's website, http://www.digestaqure.com, which found statements made about DigestaCure to be drug claims.

Recalls & Warnings

January 27, 2015

Green Coffee Bean Supplement Marketer Settles FTC Charges of Deceptive Claims

On January 26, 2015, the FTC announced that Pure Health LLC, Genesis Today, and owner of both companies, Lindsey Duncan, will pay $9 million to settle charges of deceptive weight loss claims made about the companies' green coffee bean extract products.

Recalls & Warnings

April 05, 2016

Muscle Enhancement Supplement Recalled

On April 5, 2016, Invisiblu International LLC issued a recall of one lot of the muscle enhancement supplement Continuum Labs LGD-Xtreme because it contains LGD-4033 Ligandrol. The risks of this ingredient are not known.

Recalls & Warnings

March 04, 2016

Federal Court Shuts Down Seller of Supplement Promoted for Herpes

On February 26, 2016, a federal court ordered dietary supplement company Viruxo LLC to stop selling its product Virux, which was promoted to treat herpes.

Recalls & Warnings

March 02, 2016

Seller of Hoodia and Other Supplements Admits Fraud

On March 1, 2016, The United States Department of Justice announced that David Romeo, principal of several New Jersey- based dietary supplement companies, including Global Nutrients, Stella Labs and Nutraceuticals International, LLC, has pled guilty to conspiracy to distribute three kilograms or ...

Recalls & Warnings

February 16, 2016

Work Out and Weight Supplements Contain Synthetic Amphetamine-Like Compound

On February 3, 2016, the FDA issued a warning letter to ATS Labs, LLC because labels for the company's work out and weight loss supplements CFI, Weapon-X Pre-Workout Extreme, and Lady Lean list a synthetic, amphetamine-like compound, 4-amino-2-methylpentane citrate (also called ...

Recalls & Warnings

February 16, 2016

Garden Of Life Recall Expanded

On February 13, 2016, Garden of Life LLC expanded its January 2016 recall of certain Raw Meal Organic Shake & Meal Chocolate, Original, Vanilla and Vanilla Chai products to include additional lots of these products, because they have the potential to be contaminated with ...

Recalls & Warnings

December 23, 2015

"Bee Extremely Amazed" Recalls Weight Supplements

On December 22, 2015, Bee Extremely Amazed LLC issued a voluntary recall of all lots of the following weight loss supplements, which were found to contain sibutramine and phenolphthalein: 

Recalls & Warnings

January 20, 2016

Seller of Aloe, Moringa Supplements Warned for Manufacturing Violations, Drug Claims

On January 13, 2016, the FDA issued a warning letter to Alkebulan International Services, LLC, following a facility inspection which found the company's products,Aloe Ferox and Moringa Oleifera Capsule to be adulterated because they prepared, packed, or held under conditions that ...

Recalls & Warnings

January 12, 2016

Over $400,000 Worth of Kratom Supplements Seized by U.S. Marshals

On January 6, 2016, U.S. Marshals seized nearly 90,000 bottles of dietary supplements labeled as containing kratom (brand name RelaKzpro) valued at over $400,000, from Dordoniz Natural Products LLC in South Beloit, Illinois. The action was taken at the request of the FDA.

Recalls & Warnings

February 06, 2016

Marketers of Weight Supplements AF Plus and Final Trim Violated Consumer Protection Laws, Says FTC

On January 19, 2016, the Federal Trade Commission (FTC) and State of Maine's Office of the Attorney General charged marketers of weight loss supplements AF Plus and Final Trim with violating consumer protection laws.

Recalls & Warnings

February 05, 2016

Garcinia, Green Coffee Marketers Pay $43 Million to Settle Charges of False Weight Loss Claims

Sale Slash, LLC, has agreed to pay more than $43 million to settle FTC charges it used unsubstantiated claims and fake celebrity endorsements to promote its Premium Green Coffee, Pure Garcinia Cambogia, Premium White Kidney Bean Extract, Pure Forskolin Extract, and Pure Caralluma Fimbriata Extract ...

Recalls & Warnings

May 15, 2016

Seller of Vision Supplements Warned for Drug Claims

On April 28, 2016, the FDA issued a warning letter to Macular Health, LLC.

Recalls & Warnings

May 02, 2016

Weight Loss Supplements Containing Hidden Drugs Recalled

On April 29, 2016 Making It A Lifestyle, L.L.C. issued a recall of all lots of weight loss supplements 3rd Degree, Black Gold X Advanced and Black Label X because they were found to contain undeclared sibutramine and sildenafil.

Recalls & Warnings

August 02, 2016

Seller of Whey Protein Warned for Manufacturing Violations, Drug Claims

On July 22, 2016, the FDA issued a warning letter to New Horizon Nutraceuticals, LLC, following a facility inspection which found the company's product, One World Whey Protein Power Food to be adulterated because it was prepared, packed, or held under conditions that violate Current ...

Recalls & Warnings

June 21, 2016

"Doctor Trusted" Seal and Certification Program for Dietary Supplements Misleading and Meaningless, Says FTC

SmartClick Media LLC, also doing business as Doctor Trusted, has agreed to settle Federal Trade Commission (FTC) charges that its "Doctor Trusted" seal and certificates, which appeared on some 800 websites promoting health products and dietary supplements, ...

Recalls & Warnings

June 18, 2016

Muscle Milk Protein Drinks Recalled

On June 17, 2016 HP Hood LLC issued a recall of the following Muscle Milk protein drinks because they have the potential for premature product spoilage:  

Recalls & Warnings

June 09, 2016

Nature Made Multis and B Complex Recalled Due to Salmonella, Staph Risk

On June 8, 2016 Pharmavite LLC issued a recall of the following Nature Made® multivitamin and B complex supplements because they have the potential to be contaminated with Salmonella or Staphylococcus aureus:

Recalls & Warnings

October 13, 2016

Nutrisystem Bars Recalled Due to Listeria Risk

On October 11, 2016, Nutrisystem Everyday, LLC issued a recall of one lot of its Nutricrush Chocolate Chip Cookie Dough bar because it has the potential to be contaminated with Listeria monocytogenes.

Recalls & Warnings

August 09, 2016

Liquid Multis, Vitamin D & More Recalled Due to Potential Bacterial Contamination

On August 8, 2016, PharmaTech, LLC issued a recall of twenty liquid vitamin supplements, sold under various brand names, because they have the potential to be contaminated with Burkholderia cepacia.

Recalls & Warnings

February 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

January 07, 2017

Seller of Protein and Workout Supplements Warned for Manufacturing Violations, Label Errors

On December 22, 2016, the FDA issued a warning letter to Rock Solid Nutrition, LLC, following a facility inspection which found the company's products, including  Whey Isolate (Cinnabun flavor), Pre-Pump (Massive Mango flavor)  and Strength Test to be adulterated because ...

Recalls & Warnings

April 01, 2017

Maker of Prelief, Urinozinc Prostate Health Formula Warned for Manufacturing Violations

On March 16, 2017 the FDA issued a warning letter to DSE Healthcare Solutions, LLC, following a facility inspection which found the company's products, including Prelief and Urinozinc Prostate Health Formula to be adulterated because they were prepared, packed, or held under ...

Recalls & Warnings

June 07, 2017

FDA Warns Seller of Probiotic and Omega-3 Supplements for Manufacturing Violations

On May 22, 2017, the FDA issued a warning letter to BioTE Medical, LLC following a facility inspection which found its products, including BioTE DIM, BiotTE Probiotic, BioTE Iodine Plus, and BioTE Omega 3 to be adulterated because they were prepared, packed, or held under ...

Recalls & Warnings

May 30, 2017

Beef Bone Broths Recalled

On May 26, 2017, Cauldron Soups, LLC (DBA Cauldron Broths) issued a recall of approximately 5,163 pounds of beef broth products because they were produced without the benefit of federal inspection.

Recalls & Warnings

May 26, 2017

"Allergy" Supplement Containing Ephedra Recalled

On February 7, 2017, MusclMasster, LLC (DBA The Green Herb) of Wheat Ridge, CO issued a recall of all bottles of Al-Er-G Capsules , a product promoted to help allergies, because they contain ephedra.

Recalls & Warnings

May 20, 2017

Muscle Enhancement Supplement Containing Steroid-Like Substances Recalled

On May 19, 2017, Dynamic Technical Formulations LLC issued a recall of all lots its muscle enhancement supplement Tri-Ton because it was found to contain anabolic steroid-like substances (andarine and ostarine) which are not permitted in dietary supplements.

Recalls & Warnings

July 18, 2017

Seller of "Super Strength Prostate Formula," Acai Berry Supplements & More Warned for Drug Claims

On June 30, 2017, the FDA issued a warning letter to Nature's Health Company, LLC, following a facility inspection and review of the company's website, www.natureshealthcompany.

Recalls & Warnings

October 07, 2017

Weight Loss Supplement Recalled

On October 5, 2017, Kiriko, LLC recalled recalled all lots of A1 Slim 30 capsules after FDA analysis found the products to contain sibutramine, phenolphthalein and N-Desmethyl sibutramine.

Recalls & Warnings

November 20, 2013

Another Sexual Enhancement Supplement Recalled Due To Undeclared Drugs

On November 18, 2013, Fossil Fuel Products, LLC issued a voluntary recall of sexual enhancement supplement RezzRX because it was found to contain the undeclared drugs hydroxylthiohomosildenafil and aminotadalafil.

Recalls & Warnings

November 20, 2013

OxyElite Pro Recall Expanded

On November 19, 2013, USPlabs LLC expanded its recall of OxyElite Pro products to include Raspberry Lemonade OxyELITE Pro Super Thermo Powder (4.6 oz., UPC #094922447494).

Recalls & Warnings

May 02, 2015

Maker of Garcinia, Joint Supplements and More Warned for Manufacturing Violations, Drug Claims

On March 25, 2015, the FDA issued a warning letter to JW Nutritional LLC, following a facility inspection which found the company's products, including  Vanish V2 Domestic, Mr.

Recalls & Warnings

September 13, 2014

Marketer Banned From Selling Weight Loss Products

In order to settle FTC charges of deceptive weight loss claims, John Matthew Dwyer III, the co-founder of HealthyLife Sciences, LLC, has agreed to no longer manufacture or market weight loss supplements.

Recalls & Warnings

August 26, 2014

Maker of Herbal Supplements Warned for Manufacturing Violations and Drug Claims

On August 8, 2014, the FDA issued a warning letter to EnerHealth Botanicals, LLC following a facility inspection which found the company's products, including Parasite Purge Herbal Remedy, Black Walnut Extract, Bladder Cleanse Herbal Extract, Lung Renewal Herbal Remedy, EchinOsha and Daily Immune ...

Recalls & Warnings

July 02, 2014

Protein Drink Mix Recalled Due to Salmonella Risk

On July 1, 2014, Oriya Organics, LLC voluntarily recalled Oriya Organics Superfood Protein Medley (21.2 oz) because it contains Organic Sprouted Chia Seed Powder, which has the potential to be contaminated with Salmonella.

Recalls & Warnings

May 06, 2014

Seller of Flaxseed, Ginkgo and More Warned for Manufacturing Violations and Drug Claims

On April 18, 2014, the FDA issued a warning letter to Iowa Select Herbs, LLC, following a facility inspection which found the company's products, including Flax Seed, Holy Basil, Papaya Leaf Extract, and Ginkgo Leaf Extract products, to be adulterated because they were prepared, packed, or held ...

Recalls & Warnings

May 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

March 27, 2014

Bee Pollen and Weight Loss Supplements Recalled

On March 26, 2014, Pure Edge Nutrition, LLC issued a voluntary recall of Bella Vi Insane Bee Pollen Capsules, Bella Vi BTrim Ultimate Boost, Bella Vi BTrim Max, Bella Vi Extreme Accelerator, Bella Vi Insane Amp'd, and two lots of Bella Vi Amp'd Up because they were found to contain sibutramine, ...

Recalls & Warnings

February 17, 2014

Weight Loss Supplement Recall Expanded to Include Additional Products

On February 4, 2014, MyNicKnaxs, LLC, which first issued a recall of Reduce Weight Fruta Planta, issued a recall of nine additional weight loss supplements: Magic Slim, Fruta Bio, SlimEasy, Super Fat Burning Bomb, Slim Xtreme, Meizi Evolution, Meizitang Strong Version Botanical Slimming, ...

Recalls & Warnings

February 14, 2014

Weight Loss Supplement Containing Drug Recalled

On February 4, 2014, MyNicKnaxs, LLC. issued a recall of weight loss supplement Reduce Weight Fruta Planta because it was found to contain phenolphthalein.

Recalls & Warnings

February 13, 2014

Seller of Iron, Prostate, Valerian and Other Supplements Warned For Multiple Violations and Drug Claims

On January 31, 2014, the FDA issued a warning letter to NatureAll-STF Holding, LLC, following a facility inspection which found the company's products, including Colostrum, Valerian-Plus, Wormwood, Black Walnut-Plus, Lung-Plus, Yucca-Plus (Arthro Plus), Iron Plus, MSM Plus, White Willow Plus, ...

Recalls & Warnings

December 30, 2014

Maker of Probiotic Supplement Warned for Manufacturing Violations

On December 18, 2014, the FDA issued a warning letter to Wellmill LLC, dba Vitamix, following a facility inspection which found the company's products, including Butcher's Broom powder and Lactobacillus acidophilus powder (used as ingredients in a finished product which was not named) to be ...

Recalls & Warnings

December 12, 2014

Marketers of HCG Settle FTC Charges of Deceptive Weight Loss Claims

Marketers of HCG Platinum drops have agreed to pay $1 million to settle Federal Trade Commission (FTC) charges that claims the drops could cause rapid and substantial weight loss were deceptive and not supported by scientific evidence.

Recalls & Warnings

December 05, 2014

Maker of Ginseng, Zinc, Calcium and More Warned for Manufacturing Violations

On November 20, 2014, the FDA issued a warning letter to Long Island Pharmaceuticals, LLC, following a facility inspection which found the company's products to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for dietary ...

Recalls & Warnings

December 02, 2014

Seller of Energy & Joint Supplements, Aloe, Silver and More Warned for Drug Claims

On November 24, 2014, the FDA issued a warning letter to Jansen Enterprises, LLC, dba HealthWorksUSA, following an inspection of the company's website which found statements made about Nutra Blast Natural Energy, Ionic Silver Water, Nutra Complete, and Nutra Gel to be drug claims. 

Recalls & Warnings

November 21, 2014

Weight Loss Supplements Recalled

On November 19, 2014, REFA Enterprises, LLC issued a voluntary recall of one lot each of Forever Beautiful Bee Pollen and Forever Beautiful Infinity because they were found to contain sibutramine or a combination of sibutramine and phenolphthalein.

Recalls & Warnings

November 11, 2014

Seller of Sexual, Muscle Enhancement Supplements Warned for Manufacturing Violations and Drug Claims

On August 26, 2014, the FDA issued a warning letter to GE Pharma LLC following a facility inspection which found the company's products, including Fire Burn, Fire Storm, Creatine, Amino Fire, Nitric Fire, Jet Fire, Oxy Fire, HGH, Cissus, Hydro shield, Performa-Test, Raspberry Ketones, Fire Drol, ...

Recalls & Warnings

September 30, 2015

Weight and Energy Supplement Contains Synthetic "Amphetamine"

On September 21, 2015, the FDA issued a warning letter to TruVision Health LLC. because the company's supplement tru Weight & Energy lists a synthetic, amphetamine-like compound, AMP (also called 1,3-dimethylbutylamine or DMBA) on product labels. 

Recalls & Warnings

July 25, 2015

Weight Supplement Found to Contain Three Drugs

On July 23, 2015 Life & More, L.L.C. issued a voluntary recall of 783 bottles from one lot of Akttive High Performance Fat Burner Gold weight loss capsules because they were found to contain the undeclared drugs sibutramine, desmethylsibutramine, and phenolphthalein.

Recalls & Warnings

June 03, 2015

Maker of B-12 Energy Supplement Warned for Manufacturing Violations

On May 15, 2015, the FDA issued a warning letter to LiquidCapsule Manufacturing, LLC.

Recalls & Warnings

October 30, 2014

Supplement Maker Warned for Manufacturing Violations

On October 21, 2014, the FDA issued a warning letter to DNG Trading & Milling, LLC, following a facility inspection which found the company's products to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for dietary ...

Recalls & Warnings

October 24, 2014

Shark Cartilage Supplement Recalled

On October 17, 2014, AMS Health Sciences, LLC issued a voluntary recall of one lot of Saba Shark Cartilage Complex because it has the potential to be contaminated with Salmonella.

Recalls & Warnings

February 07, 2013

Growth Factor Supplement For "Size, Strength and Stamina" Recalled Due To Potential Contamination

On January 2, 2013, EonNutra, LLC issued a voluntary recall of specific batches of Soto Supplements Growth Factor Complex 200 GFC 200 (2 fl oz.) liquid dietary supplement due to potential bacterial contamination.

Recalls & Warnings

January 30, 2013

Maker of Cold and Flu Supplement Warned For Making Drug Claims

On January 24, 2013, the FDA and FTC jointly issued a warning letter to Flu and Cold Defense LLC, after a review of the company's website and marketing materials found statements made about the cold and flu dietary supplement GermBullet to be drug claims.

Recalls & Warnings

January 28, 2013

Recall: Male Sexual Enhancement Supplement Found to Contain Prescription Drug

On January 24, 2013, D&S Herbals, LLC, dba Freedom Trading, announced a voluntary recall of one lot of the male sexual enhancement dietary supplement Super Power because it was found to contain undeclared sildenafil.

Recalls & Warnings

January 24, 2013

Food for Health Warned for Manufacturing Violations and Drug Claims on Supplements

On October 5, 2012, the FDA issued a warning letter to Food for Health International, LLC following a facility inspection which found the company's products, including Activz brand Vitamin D, Potassium Iodine, Organic Vitamin C, Whole 9 (a fruit and vegetable meal replacement shake) Control and VMA ...

Recalls & Warnings

February 21, 2013

Pet Supplement Company Issues Recall Due To Potential Bacterial Contamination

On February 20, 2013, animal supplement company Nutri-Vet, LLC issued a recall of Nutri-Vet and NutriPet Chicken Jerky Products because they may be contaminated with Salmonella.

Recalls & Warnings

February 20, 2013

FDA Warns USPLabs For Adulteration and Drug Claims

On December 4, 2012 the FDA issued a warning letter to USPLabs, LLC following facility inspections which found the company's products, including dietary supplements Jacked3d, OxyElite Pro, Prime, and Super Cissus, to be adulterated because they were prepared, packed, or held under conditions that ...

Recalls & Warnings

February 15, 2013

FDA Seizes Weight Loss Supplements Containing Undeclared Drug

On Feb. 14, 2013, U.S. Marshals acting on behalf of the FDA seized weight loss supplements from Globe All Wellness, LLC which were found to contain the undeclared drug sibutramine hydrochloride.

Recalls & Warnings

March 08, 2012

Rx Drugs Found in Weight Loss and Enhancement Supplements

On February 6, 2012, FDA issued a letter to Globe All Wellness, LLC warning that two of their products contain undeclared prescription drugs.

Recalls & Warnings

November 06, 2012

Recall of "Bee Pollen" Supplement Found to Contain Drug

On October 24, 2012, Zi Xiu Tang Success, LLC issued a voluntary recall of Classic Zi Xiu Tang Bee Pollen Capsules and Ultimate Formula Capsules because the supplements contain the undeclared drug sibutramine.

Recalls & Warnings

September 26, 2012

Maker of Eye Health Supplements Warned for Drug Claims

On September 18, 2012, the FDA issued a warning letter to EyeScience Labs, L.L.C. because statements made about the company's Macular Health Formula, Dry Eye Formula and Diabetic Vision Formula supplements were found to constitute drug claims.

Recalls & Warnings

July 23, 2013

Weight Loss Supplements Containing Undeclared Drugs Recalled

On July 19, 2013, Herbal Give Care LLC issued a voluntary recall of all lots of weight loss supplements Esbelin siloutte te and Esbelin siloutte Herbal Blend with L-Carnitine because they were found to contain undeclared sibutramine, N-desmethylsibutramine, and N-di-desmethylsibutramine.

Recalls & Warnings

October 27, 2013

Ingredient In Workout Supplements May Be Unsafe, FDA Warns

On October 11, 2013, the FDA directed USP Labs, LLC to cease distribution of workout supplement OxyElite Pro and and muscle-building supplement VERSA-1, which are labeled as containing the ingredient aegeline, or N-[2-hydroxy-2(4-methoxyphenyl) ethyl]-3-phenyl-2-propenamide.

Recalls & Warnings

October 01, 2013

Three Sexual Enhancement Supplements Containing Undeclared Drug Recalled

On September 24, 2013, Haute Health, LLC issued a voluntary recall of all lots of sexual enhancement supplements Virilis Pro, PHUK and Prolifta, because they were found to contain sildenafil.

Recalls & Warnings

September 15, 2013

Creatine Powder Containing DMAA Recalled

On September 12, 2013, Ge Pharma, LLC issued a recall of grape and fruit punch flavors of Creafuse Powder because they contain 1,3 dimethylamylamine (DMAA).

Recalls & Warnings

August 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

August 27, 2013

Immune Supplement Recalled Due To Undeclared Milk

On August 23, 2013, Reaction Nutrition, LLC issued a voluntary recall of immune support supplement LIVE CLINICAL 90 CAPS because it contains undeclared milk.

Recalls & Warnings

May 10, 2013

Seller Of Sexual Enhancement and Hormonal Balance Supplements Warned For Manufacturing Violations

On April 26, 2013, the FDA issued a warning letter to Pristine Bay, L.L.C.

Recalls & Warnings

May 05, 2003

FDA Reports False Claims by Maker of HGH Supplement

On April 30, 2003, the Food and Drug Administration (FDA) announced that Nature's Youth, LLC, of Centerville, Mass., has completed its voluntarily destruction of approximately 5700 boxes (each containing a 30-day supply) of its misbranded product, "Nature's Youth hGH.

Recalls & Warnings

January 11, 2012

Herbal Extract Company Warned by FDA of Making Drug Claims

On January 3, 2012, the U.S. FDA sent a Warning Letter to Herbal Extract Plus, LLC regarding legal violations for claiming its herbal products can cure or prevent diseases.

Recalls & Warnings

March 04, 2011

Recall of "Raw" Vitamin C Supplement Containing Soy

The FDA posted a notice dated March 2, 2011 from Garden of Life, LLC regarding that company's voluntary recall of its Raw Vitamin C supplement because it may contain undeclared soy proteins.

Recalls & Warnings

January 04, 2011

Weight Loss Supplement Containing a Drug Can Cause Serious Adverse Events, Warns FDA

On December 31, 2010 the U.S. FDA warned consumers not to use Fruta Planta weight loss products because they contain sibutramine, a drug withdrawn from the market in December 2010 for safety reasons.

Recalls & Warnings

December 14, 2010

FDA Warns Consumers to Avoid Man Up Now Capsules

On December 14, 2010, the U.S. FDA warned consumers not to use Man Up Now capsules, marketed as a dietary supplement for sexual enhancement, because they contain a variation of an active drug ingredient found in Viagra that can dangerously lower blood pressure.

Recalls & Warnings

November 06, 2009

FDA Warns that "Stiff Nights" Enhancement Supplement Contains Undeclared Drug

On November 5, 2009 the U.S. Food and Drug Administration (FDA) warned consumers that Stiff Nights, a product marketed as a dietary supplement for sexual enhancement, contains an ingredient that can dangerously lower blood pressure and is illegal.

Recalls & Warnings

September 12, 2006

U.S. Marshalls Seize Supplements Promoted as Drugs

On September 6, 2005, the U.S. Food and Drug Administration (FDA) announced that, at its request, U.S. Marshals seized quantities of Ellagimax capsules, Coral Max capsules, Coral Max without Iron capsules, and Advanced Arthritis Support capsules distributed by Advantage Nutraceuticals L.L.C.

Recalls & Warnings

May 13, 2009

Body-Building Supplements Confiscated by FDA for Adulteration

On May 11, 2009, the U.S. FDA announced that U.S. Marshalls seized more than 23,300 bottles of three dietary supplement products distributed by LG Sciences LLC, of Brighton, Mich.

Recalls & Warnings

July 30, 2008

Recall of Viapro Capsules Due to Potentially Harmful Ingredient

The U.S. FDA has posted a release noting that EG Labs, LLC announced a nationwide voluntary recall on July 23, 2008 of all lots of its supplement product sold under the brand name, Viapro, in 375mg capsules.

Recalls & Warnings

April 07, 2008

Federal Agents Seize Nearly $1.3 Million of Illegal Dietary Supplements

On April 4, 2008 the U.S. FDA announced that, at its request, U.S. Marshals had seized more than $1,301,712 of dietary supplements from LG Sciences, LLC, of Brighton, Mich.

Recalls & Warnings

March 13, 2006

FDA Warns About Steroid Products Sold as Dietary Supplements

On March 9, 2006, the U.S.

Recalls & Warnings

January 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

July 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

November 03, 2009

Recall of 65 Dietary Supplements That May Contain Steroids

On November 3, 2009, as part of its ongoing cooperation with the Food and Drug Administration ("FDA"), Bodybuilding.

Recalls & Warnings

November 29, 2012

Sensa Settles Second False Advertising Lawsuit

On November 27, 2012, Sensa Products LLC, maker of the Sensa Weight Loss System, announced it agreed to settle a false advertising lawsuit filed by the Nutritional Supplemental Task Force in California, without an admission of guilt.

Recalls & Warnings

April 26, 2013

Seller of Immune, Cholesterol, Liver and Blood Sugar Products Warned For Drug Claims

On March 20, 2013, the FDA issued a warning letter to Birkdale Medicinals LLC, following a review of the company's website which found statements made about Birkdale products, including Immune Response 247, Cholestat, Silymarin 81 and LevelStat, to be drug claims.

Recalls & Warnings

April 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

February 21, 2013

FDA and FTC Warn: Supplements Cannot Prevent, Treat Or Cure Cold And Flu

On February 11, 2013, the FDA and the Federal Trade Commission (FTC) jointly issued warning letters to three dietary supplement companies regarding their potential illegal marketing of products to prevent, treat or cure flu virus.

Recalls & Warnings

August 20, 2013

Weight Loss Supplement Formulas For Men and Women Recalled Due To Undeclared Drugs

On August 16, 2013, Herbal Give Care LLC issued a voluntary recall of all lots of weight loss dietary supplements Esbelder man, Esbelder fem and Esbelder siloutte because they were found to contain the undeclared drugs sibutramine, N-desmethylsibutramine, and N-di-desmethylsibutramine.

Recalls & Warnings

October 03, 2014

Seller of Green Tea, Prostate, Pain Supplements and More Warned for Manufacturing Violations and Drug Claims

On July 25, 2014, the FDA issued a warning letter to AMS Health Sciences, LLC following a facility inspection which found the company's products, including saba ACE, UROPOWER, UROSure, Digest-Eze, Shark Cartilage, Colloidal Silver, and Mobilite to be adulterated because they were prepared, packed, ...

Recalls & Warnings

September 26, 2014

Seller Warned for Promoting Essential Oils to Treat Flu, MRSA, Measles and More

On September 22, 2014, the FDA issued a warning to doTERRA International, LLC.

Recalls & Warnings

May 30, 2015

Seller of Omega-3, Probiotics & SuperFoods Warned for Manufacturing Violations, Drug Claims

On May 4, 2015, the FDA issued a warning letter to Dr. Dennis Black, LLC.

Recalls & Warnings

November 06, 2014

Seller of Prostate, Heart Supplements and More Warned for Drug Claims

On October 9, 2014, the FDA issued a warning letter to Health Research Laboratories, LLC/New World Health, following a review of the company's websites, which found statements made about AtheChel Advanced, Betarol, BioTherapex, Omega-3 Cardio Plus, RejuvaLifeRx, and Ultimate Health Formula to be ...

Recalls & Warnings

January 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

November 11, 2013

Workout Supplement OxyElite Pro Recalled After Being Linked to Serious Liver Illness

On November 10, 2013, the FDA announced that USPLabs LLC is recalling workout supplements OxyElite Pro Super Thermo capsules, OxyElite Pro Ultra-Intense Thermo capsules and OxyElite Pro Super Thermo Powder because they have been linked to a number of cases of acute non-viral hepatitis, one of which ...

Recalls & Warnings

December 06, 2013

Weight Loss Supplement Claims Challenged

On November 27, 2013, the National Advertising Division (NAD) recommended HealthyLife Sciences, LLC, modify or discontinue the use of certain claims made about the company's weight loss supplement Healthe Trim.

Recalls & Warnings

June 23, 2017

FDA Warns Seller of Menopause, Sexual Enhancement, Prostate Supplements and More For Manufacturing Violations

On May 26, 2017 the FDA issued a warning letter to Star Health & Beauty LLC, following a facility inspection which found the company's products, including Nu Essentials Royal Jelly Capsules, NuMan Male Enhancement Capsules, Star's Male Potency Tonic, NuGen HP, She Max HP, and V Max ...

Recalls & Warnings

August 18, 2017

FDA Warns Consumers Not to Use Certain Liquid Multis, Vitamin D, and Other Supplements Due to Potential Bacterial Contamination

On August 11, 2017, the FDA advised the public not to use any liquid drug or dietary supplement products manufactured by PharmaTech LLC of Davie, Florida, and labeled by Rugby Laboratories, Major Pharmaceuticals, and Leader Brands, because they have the potential to be contaminated with ...

Recalls & Warnings

February 25, 2017

Radio "Infomercials" for Cognitive and Joint Health Supplements Deceived Consumers, Says FTC

On February 22, 2017, the Federal Trade Commission and the Maine Office of the Attorney General announced a complaint the marketers of CogniPrin and FlexiPrin, charging that they made misleading claims about the supplements in radio infomercials deceptively formatted as talk shows.

Recalls & Warnings

February 01, 2016

Garden of Life Shakes and Meals Recalled Due to Salmonella Risk

On January 29, 2016, Garden of Life LLC issued a recall of certain Raw Meal Organic Shake & Meal Chocolate, Original, Vanilla and Vanilla Chai products because they have the potential to be contaminated with Salmonella.

Recalls & Warnings

December 16, 2015

Maker of Red Yeast Rice, St. John's Wort, Valerian and More Warned for Manufacturing Violations, Drug Claims

On December 2, 2015, the FDA issued a warning letter to Nature's Health, LLC, following a facility inspection which found the company's product, including Ginkgo & Rhodiola, Blood Sugar Balance IV, Cinnamon Extract, Choles-Balance Red Yeast Extract, Lecithin, Milk Thistle Seed Extract, ...

Recalls & Warnings

November 07, 2015

Seller of "NaturalDoctor" Vitamin C, Echinacea and More Warned for Manufacturing Violations

On October 16, 2015, the FDA issued a warning letter Sound Healing Arts, PC, dba Grounds for Tea, LLC, following a facility inspection which found the company's products, including  NaturalDoctor Vitamins C & K3, NaturalDoctor Goldenseal & Echinacea Plus, NaturalDoctor Centella ...

Recalls & Warnings

October 28, 2015

GNC Accused of Selling Supplements with Unlawful Ingredients

On October 22, 2015, Oregon Attorney General Ellen Rosenblum filed a lawsuit against supplement retailer GNC, alleging that the company sold products that were adulterated with BMPEA and picamilon, which are not lawful dietary supplement ingredients.

Recalls & Warnings

October 08, 2015

FDA Warns Seller of Omega-3 "Concussion" Supplement for Drug Claims

On October 1, 2015, the FDA issued a warning letter to MPH Nutrition, LLC, following a review of the company's website which found statements made about  Re:Mind Recover, a supplement promoted for recovery from concussions, to be drug claims which are not permitted for supplements.

Recalls & Warnings

August 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

February 27, 2018

Dog Treats, Food Recalled Due to Salmonella, Listeria Risk

The following dog treats and dog food are being recalled because they have the potential to be contaminated with Listeria monocytogenes or Salmonella, which can cause illness in pets who consume these products, as well as in pet owners who handle the contaminated products or touch ...

Recalls & Warnings

December 01, 2017

Health Research Labs Agrees to Settle FTC Charges of False Claims, Deceptive Marketing of BioTherapex and NeuroPlus

On November 30, 2017, the FTC announced Health Research Laboratories LLC and owner, Kramer Duhon, agreed to settle charges that they made false claims about the company's products, BioTherapex and NeuroPlus.

Recalls & Warnings

April 03, 2018

FDA Issues Mandatory Recall of Salmonella-Contaminated Kratom Products

On April 2, 2018, the FDA issued a mandatory recall of all food products containing powdered kratom manufactured, processed, packed, or held by Triangle Pharmanaturals LLC because several of company's products were found to be contaminated with Salmonella.

Recalls & Warnings

April 02, 2018

NutriZone Kratom Supplements Recalled Due to Salmonella Risk

On March 10, 2018, NutriZone, LLC issued a recall of certain kratom-containing powder products because they have the potential to be contaminated with Salmonella.

Recalls & Warnings

March 31, 2018

Nutrition Bars Sold at Whole Foods and Online Recalled

On March 26, 2018, eBars LLC, issued a recall of their Protein Bars, Snack Bars, and Kids Bars because they may contain undeclared peanuts and/or almonds.

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