Showing Results for Joint Health

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Product Review

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

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

CL Answer

What are the side effects of glucosamine and chondroitin?

Learn the side effects of glucosamine and chondroitin supplements for joint health and joint pain, including stomach upset, headache, and many others. ConsumerLab.com's answer explains.

Product Review

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

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

CL Answer

What is BPC-157, what is it used for and is it safe?

Find out about BPC-157, including what it's promoted for and if it is safe.

CL Answer

Is hyaluronic acid helpful for osteoarthritis?

Hyaluronic acid supplement information including joint pain, osteoarthritis, clinical evidence, dosage and more.

CL Answer

Does taking curcumin and boswellia together increase their individual anti-inflammatory effects?

Find out if taking boswellia and curcumin together can increase their individual anti-inflammatory effects. ConsumerLab.com's answer explains.

CL Answer

My dog is getting older and his veterinarian recently recommended giving him a glucosamine supplement for his joints. Has ConsumerLab.com tested these, or other supplements for pets?

Find out our test results on glucosamine for dogs and cats as well as other supplements for pets.

CL Answer

I have to be careful about my sodium intake. Could my glucosamine and chondroitin supplement contain hidden sodium?

Find out if glucosamine and chondroitin supplements contain hidden sodium and why.

CL Answer

Does collagen taken as a supplement help with arthritis? I'm seeing it in products for joint health.

Learn more about collagen supplements, including evidence from clinical studies on arthritis and muscle strength and safety.

CL Answer

What is UC-II and does it help joints?

What is UC-II (undenatured type 2 collagen - InterHealth Nutraceuticals) and do clinical studies show that it works for joint health?

News Release

2/25/2023

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.

CL Answer

Which supplements help for osteoarthritis of the hip?

Supplements for hip pain and osteoarthritis, such as SAMe, ginger and collagen, may help or reduce pain.

CL Answer

Does glucosamine raise "bad" LDL cholesterol?

Learn more about the link between glucosamine and cholesterol, including evidence from clinical studies.

News Release

2/24/2023

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.

CL Answer

Which supplements can help with arthritis?

Learn more about collagen supplements for joint health, including evidence from clinical studies on arthritis and muscle strength and safety.

News Release

2/25/2022

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

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

CL Answer

Are vitamins and supplements from Canada of better quality because they are licensed?

Find out if Canadian vitamins and supplements are better quality because they are licensed, what it means to for a product to have an Natural Product Number (NPN) in Canada, and if vitamins and supplements in Canada are tested for quality and purity. ConsumerLab.com's answer explains.

CL Answer

Is bromelain a good alternative to NSAIDs, like ibuprofen, for muscle or joint pain?

Do bromelain supplements have benefits? Learn more about its safety, and if it is a good alternative to NSAIDs like ibuprofen.

CL Answer

Which supplements should be taken with food?

Find out which supplements should be taken with food, including vitamins A, D, E, and K, fish oil, and CoQ10.

News Release

2/24/2022

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).

CL Answer

Do Vital 3 collagen drops really help for joint pain?

Learn more about Vital 3 collagen drops withundenatured type II collagen, and if they can help joints move better and feel better.

Product Review

Maca Supplements Review

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

Recalls & Warnings

11/28/2022

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

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

CL Answer

I was told I have a MTHFR gene mutation. Do I need to take methylated forms of B vitamins, such as methylfolate and methylcobalamin?

MTHFR gene mutation can impact B vitamin bioavailability. Learn more about this and which deficiencies are more likely to occur.

CL Answer

Can bloodroot or "black salve" treat skin cancer? Is it safe?

Bloodroot salve and black salve made from bloodroot and zinc - are they effective and safe treatments for skin cancer? ConsumerLab.com's answer explains.

News Release

8/27/2021

ConsumerLab Tests Reveal Best Joint Health Supplements for People and Pets

White Plains, New York, August 27, 2021 — Joint health supplements with ingredients such as glucosamine, chondroitin, MSM, boswellia, collagen and turmeric are often promoted to relieve joint pain or slow the progression of osteoarthritis.

News Release

2/26/2021

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

2/25/2021

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

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

Recalls & Warnings

3/09/2022

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

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

Product Review

Collagen Supplements Review

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

CL Answer

I've read about several different forms of SAMe. Is one form better than another?

Learn about the various types of SAMe (S-adenosyl-L-methionine) supplements, along with their benefits for hormones & cell membrane health.

CL Answer

What is Omega XL and does it work?

What is Omega XL (distributed by Great Health Works) and does it work? Described as a "highly concentrated Omega-3 'Super Oil' supplement".

Recalls & Warnings

9/28/2022

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 ...

CL Answer

Does chuchuhuasi reduce inflammation or back pain?

Find out if chuchuhuasi, an herb from the Amazon rainforest, can decrease inflammation or reduce back pain. ConsumerLab.com's answer explains.

CL Answer

What are the health benefits of andrographis? Can it treat colds, help with joint pain, or other conditions, and is it safe?

Learn about the health benefits of andrographis, whether it can help relieve cold symptoms, reduce pain and stiffness of osteoarthritis or rheumatoid arthritis, decrease symptoms of ulcerative colitis, or slow the growth of cancer. See the clinical evidence for the branded andrographis extract ParActin. Plus, learn about dosage, side effects and drug interactions with andrographis.

Recalls & Warnings

5/09/2013

Joint Health Supplement Recalled for Undeclared Allergens

On May 1, 2013, XYMOGEN issued a voluntary recall of the joint health supplement artriphen, because it contains undeclared soy and milk allergens.

Recalls & Warnings

9/25/2018

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

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

Recalls & Warnings

5/18/2023

EarthLab, Inc. Warned for Promoting Green Tea, Curcumin, Elderberry & More to Treat Stroke, Cancer & Flu

On April 27, 2023, the FDA issued a warning letter to EarthLab, Inc., dba Wise Woman Herbals, following inspection of the company’s website which found statements about the company’s Green Tea Solid Extract, Curcuma Spp.

Recalls & Warnings

2/11/2020

FTC Sues Two Companies Selling Bone Health and Joint Pain Supplements

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

Recalls & Warnings

9/03/2019

Federal Court Shuts Down Two Supplement Companies Selling Weight, Joint Health and Other Supplements

On September 3, 2019, a U.S. District Court entered a consent decree of permanent injunction against Basic Reset and Biogenyx, two Tennessee-based companies that sell dietary supplements and other product promoted for health benefits.

CL Answer

What are the symptoms of vitamin D deficiency?

Learn about the symptoms of vitamin D deficiency, such as soft or weak bones, bone, joint and muscle pain, depression, insomnia, hair loss and others, and find out how much vitamin D you need. ConsumerLab.com's answer explains.

CL Answer

Do collagen supplements impact cholesterol levels or reduce risk factors for atherosclerosis?

Collagen has been studied for its effects on cholesterol levels and atherosclerosis risk factors, but its effects are still not clear.

CL Answer

Does urolithin A reduce age-related muscle decline or improve osteoarthritis?

Find out if urolithin A may improve age-related muscle decline and learn about its safety.

CL Answer

Are there any serious side effects with Lovaza or Epanova (prescription fish oil)? If so, would these also apply to generic versions of these drugs and to fish oil supplements?

Understand the side effects of prescription fish oil like Lovaza and Epanova, and find out if the generic fish oils are effective and safe.

Recalls & Warnings

8/08/2022

Woman Pleads Guilty for Selling and Promoting Products to Treat COVID-19

On July 27, 2022, Diana Daffin, owner of Savvy Holistic Health pleaded guilty to selling products with claims they could treat COVID-19 and promised “Immunity for Humans.” The products were sold under the HAMPL brand name.

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

6/02/2022

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

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

Recalls & Warnings

11/21/2022

Healthy Sense and People’s Choice Multis Recalled

On November 17, 2022, Mason Vitamins Inc.

CL Answer

What are the health benefits of serrapeptase?

Serrapeptase is a proteolytic enzyme. Learn more about its health effects, including whether evidence supports its use for pain, inflammation, and heart health.

CL Answer

Do any supplements or diets help prevent or treat osteoporosis?

If you have osteoporosis, you may be interested in supplements or diets for bone health. Find out which can increase bone strength and density.

Recalls & Warnings

7/31/2018

FDA Warns Seller of Joint Health and Cholesterol Supplements

On July 13, 2018, the FDA issued a warning letter to GC Natural, following a facility inspection which found a number of the company's products, including Red Pyrola Plus + Advanced Joint Formula Capsules, CSDP GOLD Capsules, Rejeune Optimal Kidney & Liver Support Extract balls, C.

Recalls & Warnings

9/19/2018

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

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

Recalls & Warnings

11/28/2022

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

12/29/2022

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

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

Recalls & Warnings

7/14/2022

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 ...

CL Answer

Do any supplements help treat or reduce the pain of plantar fasciitis (heel pain)?

Plantar fasciitis causing heel pain has, in rare cases, been reported as a symptom of vitamin D deficiency. Other supplements that have been proposed to help include vitamin C, zinc, curcumin (from turmeric), bromelain, collagen and glucosamine. Find out what the evidence shows, and what other treatments may help.

Recalls & Warnings

12/08/2020

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.

News Release

2/25/2020

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

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

Recalls & Warnings

1/12/2021

FDA Warns Seller of Turmeric, Ashwagandha, Glucosamine, and More

On December 18, 2020, the FDA issued a warning letter to Reddy Naturals following a review of the company's website, which found statements made about the company's products Glycostasis, Glucosamine Curcumin, Turmeric 50, Turmeric Curcumin, Cetyl Curcumin, Ashwagandha, Huruli, ...

CL Answer

3 Tips to Prevent Powdered Supplements from Clumping

Learn more about how powdered supplements compare to capsules and if clumping is worrisome.

Recalls & Warnings

9/08/2020

Holistic Healthy Pet Warned for Drug Claims

On August 25, 2020, the FDA issued a warning letter to Savvy Holistic Health dba Holistic Healthy Pet following a review of the company's website, which found statements made about some of the company's products, including Doctor's Best for Your Pets, Savvy Holistic Health Pet Essences, ...

Recalls & Warnings

1/30/2018

Limbrel for Osteoarthritis Recalled Due to Risk of Adverse Effects

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

Recalls & Warnings

1/25/2018

Bulletproof Collagen Protein Recalled

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

Recalls & Warnings

1/12/2021

FDA Warns Seller of Joint and Hair Loss Products

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

Recalls & Warnings

12/15/2022

Beware of Supplements, Homeopathic Products Promoted to Treat Flu, Says FDA

On December 13, 2022, the FDA warned consumers to beware of supplements and homeopathic products, as well as nasal sprays, sanitizers and other products that promise to prevent or treat the flu.

Recalls & Warnings

3/30/2019

FDA Warns Seller of Reishi, Joint Supplements, Ginseng & More for Pesticides, Other Violations

On March 12, 2019, the FDA issued a warning letter to Yanqing "Michael" Li and Chang Su, owners of the website http://www.woohoonatural.

Recalls & Warnings

12/09/2021

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 ...

CL Answer

Does silica have health benefits? What is BioSil, and can it really increase collagen production and strengthen hair, skin, nails and bones?

Information about the health effects of silica (silicon dioxide) and orthosilicic acid (an ingredient in BioSil), including whether these forms of silicon can really increase collagen production, thicken hair, strengthen nails & bones.

Recalls & Warnings

12/05/2019

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

11/10/2020

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

3/04/2021

Federal Court Bars Confidence USA from Selling Supplements

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

Recalls & Warnings

9/25/2018

FDA Warns Seller of Digestive Enzyme Supplements

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

News Release

10/04/2019

ConsumerLab Tests Reveal Best Collagen Supplements for Wrinkles and Joints

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

News Release

5/15/2019

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.

Recalls & Warnings

1/16/2014

Joint Health Supplement Contains Dangerous Drugs, FDA Warns

On January 15, 2014, the FDA warned consumers not to buy or use joint health supplement Pro ArthMax (by Human Science Foundation) because it was found to contain multiple drugs, including diclofenac, ibuprofen, naproxen, indomethacin, nefopam, and chlorzoxazone.

Recalls & Warnings

12/11/2020

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

6/16/2020

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.

News Release

2/25/2019

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

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

Recalls & Warnings

10/06/2020

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

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

News Release

10/02/2018

Best Joint Health Supplements Identified -- ConsumerLab Tests Glucosamine, Chondroitin, MSM and Boswellia Supplements for People and Pets

White Plains, New York, October 2, 2018 — Do joint health supplements with ingredients such as glucosamine, chondroitin, Boswellia, and MSM really relieve joint pain or slow the progression of osteoarthritis? If so, which products are best? To find out, ConsumerLab recently tested popular ...

Recalls & Warnings

7/16/2019

FDA Warns Seller of Magnesium and CBD

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

Recalls & Warnings

4/17/2020

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.

News Release

3/27/2018

You Can't Always Rely on Bone Broth Labels -- ConsumerLab Tests Reveal How Much Protein, Collagen and Sodium Is Really In Bone Broths

White Plains, New York, March 27, 2018 — Bone broth is promoted as a natural source of collagen, an immune-booster, and a remedy for everything from joint pain to wrinkles.

Recalls & Warnings

4/17/2020

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

6/02/2020

Sundial Herbal Ordered to Halt Distribution of Products

On June 1, 2020, a New York federal judge filed an order against two individuals doing business as Sundial Herbal Products to stop the company from distributing its products, which were found to be misbranded and promoted as drugs.

Recalls & Warnings

4/14/2020

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

5/30/2017

Maker of Collagen Supplement Warned for Manufacturing Violations

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

Recalls & Warnings

11/29/2016

Seller of Mineral, Joint Supplements and More Warned for Manufacturing Violations, Drug Claims

On July 1, 2016, the FDA issued a warning letter to BioGenyx-Basic Reset, following a facility inspection which found the company's products, including Ionyte, Aqualyte, Beta Factor, Bee Gold and Primo Java to be adulterated because they were prepared, packed, or held under ...

Recalls & Warnings

8/31/2016

Seller of Joint Supplement Warned for Manufacturing Violations, Drug Claims

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

Recalls & Warnings

9/14/2016

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

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

Recalls & Warnings

9/19/2018

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

12/27/2019

Federal Court Shuts Down Three Supplement Companies With Serious Manufacturing Violations

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

Recalls & Warnings

8/21/2019

Large Multivitamin, Calcium Pills Can Be a Choking Hazard for Older Adults

Approximately 19% of adverse events associated with dietary supplements involve swallowing problems, especially choking, and this is mostly likely to occur in adults age 65 or older, according to a new report published in the Annals of Internal Medicine.

Recalls & Warnings

1/17/2018

Joint and Pain Relief Product Contains Undeclared Drug

On January 17, 2018 Health Canada warned consumers that Linsen Double Caulis Plus, a supplement for joint pain, was found to contain the undeclared drug dexamethasone.

News Release

2/25/2018

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

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

News Release

2/24/2017

Vitamin D Supplements Maintain Top Spot in Popularity, as Probiotics Surpass Multivitamins to #4 Behind Fish Oil and CoQ10 in Latest ConsumerLab.com Survey

White Plains, New York, February 24, 2017 — A recent survey of over 9,505 people who use dietary supplements shows the most popular dietary supplement to be vitamin D, followed by fish oil, CoQ10, probiotics, and multivitamins.

News Release

7/29/2016

ConsumerLab.com Discovers Problems with Most Multivitamins for Dogs and Cats

White Plains, New York, August 2, 2016 — After discovering in January that none of the three pet multivitamins it had purchased and tested contained all of what was listed on the labels, ConsumerLab.

News Release

6/03/2016

What Works for Joint Health? ConsumerLab.com Reviews Glucosamine, Chondroitin, MSM and Boswellia Supplements for People and Pets

White Plains, New York, June 3, 2016 — Do popular joint health supplements with ingredients such as glucosamine, chondroitin, Boswellia, and MSM really work to relieve pain or slow the progression of osteoarthritis? And, with so many to choose from, which supplements are best? To find out, ...

Recalls & Warnings

12/19/2013

Maker of Joint Health Supplements Warned for Manufacturing Violations

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

News Release

2/26/2014

Mislabeling of Some Joint Health Supplements with Glucosamine, Chondroitin, Boswellia, and MSM According to ConsumerLab.com -- 38 Supplements Tested, Including Products for Dogs and Cats --

White Plains, New York, February 26, 2014 — Glucosamine, chondroitin, Boswellia, and MSM are popular dietary supplement ingredients for treating symptoms of osteoarthritis — worn joint cartilage.

News Release

5/08/2012

Lead Contamination and Mislabeling in Joint Health Supplements with Glucosamine, Chondroitin, and MSM According to ConsumerLab.com

White Plains, New York, May 8, 2012 — Glucosamine, chondroitin, and MSM are popular dietary supplements for treating symptoms of osteoarthritis — worn joint cartilage.

Recalls & Warnings

11/25/2017

Seller of "BounceBack" Joint Supplement and Others Products Warned for Drug Claims

On November 14, 2017, the FDA sent a warning letter to Mannatech Incorporated following a facility inspection that found the products BounceBack, MannaBears, ImmunoSTART, TruSHAPE, and Catalyst to be in violation of the Current Good Manufacturing ...

Recalls & Warnings

2/25/2017

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

5/15/2018

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

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

Recalls & Warnings

12/12/2018

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

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

Recalls & Warnings

12/05/2018

Seller of Cold and Flu Supplements, "SuperFood" & More Warned by FDA

On October 30, 2018, the FDA issued a warning letter to American Botanical Pharmacy following a review of the company's website (www.herbdoc.com) and Facebook page, which found statements made about some of its products to be drug claims.

Recalls & Warnings

12/01/2018

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

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

Recalls & Warnings

8/29/2017

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

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

Recalls & Warnings

12/19/2020

FDA Finds Unapproved Drugs in Many Weight Loss and Sexual Enhancement Products Sold Online

On December 18, 2020, the FDA warned consumers that certain products promoted for weight loss, body building, sexual enhancement, pain relief, sleep, and other uses because may contain harmful ingredients.

Recalls & Warnings

10/18/2017

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

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

Recalls & Warnings

1/21/2018

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.

News Release

2/16/2011

Some turmeric and curcumin supplements fail quality review -- ConsumerLab.com finds 20% of turmeric supplements selected for review deliver less than 15% of promised compounds

WHITE PLAINS, NEW YORK — FEBRUARY 16, 2011 — Supplements containing the herb turmeric or its key compound, curcumin, have become popular in the U.S. ConsumerLab.com cautioned today that two out of ten turmeric products recently selected for quality testing were found to provide only 7.

News Release

7/10/2009

Nine joint health supplements fail ConsumerLab.com quality review -- Lead contamination, missing ingredients and other problems found in supplements for people as well as for dogs, cats and horses; Many others approved

WHITE PLAINS, NEW YORK — JULY 10, 2009 — Nine supplements for osteoarthritis that ConsumerLab.com recently selected for testing were found to be contaminated with lead, lack all or some of a key ingredient or have other quality problems.

News Release

5/19/2009

Review of Magnesium Supplements by ConsumerLab.com Shows One-Quarter Fail Quality Tests

WHITE PLAINS, NEW YORK — MAY 19, 2009 — ConsumerLab.com reported today that among twelve magnesium supplements selected for testing, only nine met quality standards. One supplement contained only 45.

News Release

4/28/2009

40% of Green Tea and Selenium Products Fail ConsumerLab.com Review of Cancer-Prevention Supplements; Lycopene Supplements Pass

WHITE PLAINS, NEW YORK — APRIL 28, 2009 — ConsumerLab.com announced results today of its Product Review of Supplements for Cancer Prevention.  Among the products that ConsumerLab.com selected for testing, quality problems were found with two out of five green tea supplements.

News Release

12/09/2008

Tests of zinc supplements by ConsumerLab.com show only some provide dosage proven to shorten colds, reduce eye disease. Lead contamination found in one product.

WHITE PLAINS, NEW YORK — DECEMBER 9, 2008 — Zinc supplements can shorten colds and reduce the progression of advanced macular degeneration, among other uses. But a new report by ConsumerLab.

Recalls & Warnings

3/13/2018

FDA Warns Seller of Milk Thistle, Chromium, Joint Supplements & More for Manufacturing Violations

On March 9, 2018, the FDA issued a warning letter to Carol Bond Health Foods following a facility inspection which found a number of the company's products, including Dolomite, Lipo Fat Fighter, ThistleX, Injuv, and Vinpocentine, to be ...

Recalls & Warnings

5/12/2018

Seller of Astaxanthin, Cinnamon, Pine Bark and More Warned for Manufacturing Violations

On March 22, 2018, the FDA issued a warning letter to Get The Tea following a facility inspection which found the company's products, including Get the Tea Astaxanthin Max, Get the Tea Colostrum Complete, and Get the Tea Pine Bark Capsules, to be adulterated because they were ...

Recalls & Warnings

6/20/2013

Glucosamine Legal Settlement Over Labeling -- Many Products Covered

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

Recalls & Warnings

5/24/2016

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

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

Recalls & Warnings

3/28/2015

Settlement Restricts Label Claims for Certain Glucosamine Supplements

On March 23, 2015 a federal judge approved a settlement agreement which will require the maker of glucosamine products (Perrigo Co.

Recalls & Warnings

11/02/2012

Maker of Joint Health, Blood Sugar, Prostate, Ginkgo Supplements and More Warned For Drug Claims, Misbranding and Adulteration

On September 10, 2012, the FDA issued a warning letter to Global Source Management & Consulting for making drug claims about the following dietary supplements: Scientific Joint Program capsules, Alpha Lipoic Acid, Healthy Blood Sugar Diabetic Support, Dr.

Recalls & Warnings

6/07/2017

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

6/06/2017

Seller of Vision, Cholesterol, Prostate Supplements and More Warned for Drug Claims

On May 25, 2017, the FDA issued a warning letter to Herbal Doctor Remedies following a facility inspection and review of the company's websites, www.herb-doc.com, www.ChinaSecretMed.com and www.theraherb.

Recalls & Warnings

10/18/2017

Total Body Nutrition Warned for Banned Stimulant in Supplements

On September 28, 2017, the FDA issued a warning letter to Total Body Nutrition following a facility inspection which found some of 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

10/25/2016

Seller of Liquid Aloe & Mineral Supplement Warned for Manufacturing Violations

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

Recalls & Warnings

4/01/2017

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

5/02/2017

Seller of Amino Acid Supplements & More Warned for Manufacturing Violations

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

Recalls & Warnings

4/04/2017

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

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

Recalls & Warnings

2/27/2018

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

1/21/2017

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

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

Recalls & Warnings

2/14/2017

Life Extension Warned for Drug Claims

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

Recalls & Warnings

9/27/2016

Seller of B Vitamins, Omega-3s and More Warned for Manufacturing Violations, Drug Claims

On September 15, 2016, the FDA issued a warning letter to Positive Power Nutrition, following a facility inspection which found the company's products, including High Energy C-Complex, Positive Vitality, Positive Performance, Positive CardioGuard, B-Complex 100, Positive Essentials, Positive ...

Recalls & Warnings

10/08/2016

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

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

Recalls & Warnings

9/06/2016

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

8/23/2016

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

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

Recalls & Warnings

8/02/2016

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

7/23/2016

Maker of "Super Food" Warned for Manufacturing Violations

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

Recalls & Warnings

2/07/2017

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

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

Recalls & Warnings

1/17/2017

Seller of Heart, Senior and Teen Supplements Warned For Drug Claims

On December 7, 2016, the FDA issued a warning letter to Esteem Products Ltd following a review of the company's website, which found statements made about its products, Cardio Life, Total Man, Total Woman, Senior Total Man, Senior Total Woman , and Total Teen to be drug ...

Recalls & Warnings

1/07/2017

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

11/20/2020

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.

News Release

11/18/2008

Adulteration Suspected with Some "Memory" Supplements -- Few Ginkgo and Huperzine Supplements Pass ConsumerLab.com Tests; Quality High for Acetyl-L-Carnitine

WHITE PLAINS, NEW YORK — NOVEMBER 18, 2008 — Tests by ConsumerLab.com of Ginkgo biloba supplements show that few products meet quality standards.

Recalls & Warnings

9/23/2014

Maker of Joint and Weight Products Warned for Hidden Drugs, Manufacturing Violations

On September 15, 2014, the FDA issued a warning letter to West Coast Laboratories, Inc., because the company's joint health supplements, Super ArthGold and Pro ArthMax, were found to contain hidden drugs.

Recalls & Warnings

5/10/2013

Protein Extract Recalled for Undeclared Allergens

On May 6, 2013, Pure Herbs Ltd. issued a voluntary recall of Protein Extract because it contains undeclared milk and soy allergens.

Recalls & Warnings

9/10/2014

Seller of Joint Pain Supplement Warned for Drug Claims

On August 24, 2014, the FDA issued a warning letter to CreAgri, Inc., following a website review, which found statements made about the company's products, including Olivenol plus Easeflex, Olivenol plus Essence Capsules, and Olivenol plus Essence Elixer, to be drug claims.

Recalls & Warnings

12/02/2014

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

8/06/2014

Seller of Mineral and Joint Supplements Warned for Manufacturing Violations and Drug Claims

On July 25, 2014, the FDA issued a warning letter to Mezotrace Corporation following a facility inspection which found the company's products, including Calcium/Magnesium Natural Minerals & Trace Elements, Calcium/Magnesium Natural Minerals & Trace Elements with Vitamin D, and Calcium/Magnesium ...

Recalls & Warnings

2/28/2013

Maker of Liquid Omega-3 Supplements Warned For Manufacturing Violations

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

Recalls & Warnings

2/13/2013

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

12/21/2016

Seller of 5-HTP, Chromium, Curcumin and More Warned for Drug Claims

On December 1, 2016, the FDA issued a warning letter to Aurora Health and Nutrition following a review of the company's website, which found statements made about its products, 5-HTP, Alpha Lipoic Acid, the Argentyn 23 product line, Artecin 90 Vegetarian Capsules, ...

Recalls & Warnings

5/02/2015

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

9/17/2013

Seller of Omega-3 and Joint Supplements Warned for Manufacturing Violations and Drug Claims

On August 29, 2013, the FDA issued a warning letter to Y.S. Health Corp.

Recalls & Warnings

8/21/2014

Seller of Joint Supplement Warned for Manufacturing Violations and Drug Claims

On July 17, 2014, the FDA issued a warning letter to Klein Laboratories, Inc.

Recalls & Warnings

4/24/2023

FTC Warns Almost 700 Companies: Unsupported Health Claims May Result in Substantial Civil Penalties

On April 13, 2023, the Federal Trade Commission (FTC) notified approximately 670 companies that market over-the-counter (OTC) drugs, homeopathic products, dietary supplements, or functional foods that they could incur significant civil penalties if they make unsubstantiated claims about the ...

Recalls & Warnings

6/17/2015

Maker of Joint Supplement Warned for Manufacturing Violations

On May 29, 2015, the FDA issued a warning letter to Total Health Advanced Nutrition, Inc.

Recalls & Warnings

6/06/2015

Joint Supplement Contains Drugs, FDA Warns

On June 5, 2015 the FDA warned consumers not to buy or use joint pain supplement Pyrola Advanced Joint Formula because it was found to contain diclofenac and chlorpheniramine. 

Recalls & Warnings

7/02/2015

Maker of Arthritis Supplement Warned for Manufacturing Violations, Drug Claims

On June 17, 2015, the FDA issued a warning letter to Desert Stream, Inc.

Recalls & Warnings

5/24/2013

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

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

Recalls & Warnings

2/28/2013

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

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

Recalls & Warnings

6/09/2020

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

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

Recalls & Warnings

12/05/2014

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

3/04/2022

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

3/01/2023

Seller of Dr. Miller’s Herbal “Detox” Teas Warned by FDA for Drug Claims

On February 3, 2023, the FDA issued a warning letter to Jackson Health & Wellness Clinic after inspection of the company’s website found statements about the company’s Dr. Miller’s Holy Tea, Dr. Miller’s Super Holy Tea, Dr. Miller’s Ultimate Tea, Dr.

Recalls & Warnings

12/01/2022

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

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

Recalls & Warnings

5/16/2015

FTC Mails Refund Checks to Nopalea Consumers

On May 15, 2015, the FTC announced it is mailing almost 500,000 checks totaling approximately $3 million to consumers who purchased the cactus-based fruit drink Nopalea (TriVita Inc).

Recalls & Warnings

4/24/2014

Arthritis Supplement Containing Multiple Drugs Recalled

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

Recalls & Warnings

2/20/2013

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

2/13/2014

FDA Warns Consumers Not To Buy or Use Arthritis Supplement

On February 13, 2014, the FDA warned consumers not to buy or use arthritis supplement Arth-Q because it was found to contain ibuprofen.

Recalls & Warnings

12/02/2014

Glucosamine Class-Action Settlement Reversed by Appeals Court

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

Recalls & Warnings

9/24/2020

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

2/02/2021

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

3/01/2013

Manufacturer of Joint, Weight Loss, Muscle Supplements and More Warned for Adulteration, Misbranding and Drug Claims

On February 4, 2013, the FDA issued a warning letter to DC Nutrition, Inc.

Recalls & Warnings

3/29/2016

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

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

Recalls & Warnings

4/17/2020

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

6/16/2020

FDA Warns Four Companies for Unsafe "Homeopathic" Injectables

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

Recalls & Warnings

2/21/2013

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

5/17/2013

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

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

Recalls & Warnings

11/21/2014

Herbal Arthritis Supplement Found to Contain Undeclared Drugs

On November 20, 2014, the FDA warned consumers not to purchase or use the herbal dietary supplement Feng Shi Ling because it was found to contain the undeclared drugs diclofenac and indomethacin.

Recalls & Warnings

5/06/2015

Joint Pain Supplements Found to Contain Diuretics, Antihistamines and Other Undeclared Drugs

On May 4, 2015, the FDA warned consumers not to buy or use the following supplements promoted for joint or back pain because they were found to contain undeclared drugs. Each was identified during an examination of international mail shipments.  

Recalls & Warnings

6/22/2021

Living Free Vitamins, Joint, Nerve and Other Supplements Recalled

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

News Release

4/24/2007

ConsumerLab.com reports improvement in quality of SAM-e supplements used for osteoarthritis and depression — Recent testing shows quality is up since studies in 2000 and 2003

WHITE PLAINS, NEW YORK — April 24, 2007 — ConsumerLab.com announced that all eight SAMe supplements that it recently selected for review passed quality testing — an improvement over tests in previous years. SAMe (S-adenosyl-methionine) is used to treat depression and joint pain.

Recalls & Warnings

11/21/2014

Seller of Diabetes, Prostate Supplements and More Warned for Manufacturing Violations, Drug Claims

On October 7, 2014, the FDA issued a warning letter to dietary supplement distributor Windmill Health Products, LLC, following a facility inspection which found the company's products, including Nutri-Betic caplets, Vita-betic caplets, ProstrinRx tablets, Polyflavanol capsules, and Glucoflex Joint ...

Recalls & Warnings

11/06/2014

Seller of Cholesterol, Arthritis Supplements and More Warned for Drug Claims

On October 17, 2014, the FDA issued a warning letter to Vitamins Direct (USA) and Golden Pride, Inc., which distribute Flexezy and Physician's Signature brands of dietary supplements, following a facility inspection which found statements made about certain supplements to be drug claims.

News Release

4/11/2007

Many arthritis supplements lack key listed ingredient — ConsumerLab.com finds chondroitin missing or low in eight supplements; Glucosamine and MSM also tested

WHITE PLAINS, NEW YORK — April 11, 2007 — Forty percent of the supplements for osteoarthritis that ConsumerLab.com recently selected for testing were found to lack all or some of their key ingredients. Osteoarthritis is the most common type of arthritis, affecting an estimated 20.

Recalls & Warnings

7/10/2021

FDA Warns Seller of Omega XL

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

Recalls & Warnings

4/30/2021

FDA Warns Seller of Fish Oil, Apple Cider Vinegar, Collagen, and Elderberry Supplements

On April 13, 2021, the FDA issued a warning letter to Orphic Nutrition following a review of the company's websites, which found statements made about the products Apple Cider Vinegar Capsules, Ashwagandha Capsules, Garcinia Cambogia Capsules, Premium Collagen Peptides Capsules, Elderberry ...

Recalls & Warnings

4/10/2021

Companies Deceived Consumers About Fish Oil for Liver Disease, Says FTC

On April 1, 2021, the Federal Trade Commission (FTC) announced that fish oil supplement manufacturer BASF SE and its U.S.

News Release

3/06/2007

ConsumerLab.com produces series of free online seminars about dietary supplements — First seminar on "joint health" now available

WHITE PLAINS, NEW YORK — MARCH 6, 2007 — ConsumerLab.com announced today that it is producing and webcasting a series of free, online audio seminars, or "webinars," that explain the use of popular types of dietary supplements.

Recalls & Warnings

11/28/2014

Seller of Herbal Extracts Warned for Manufacturing Violations, Drug Claims

On November 3, 2014, the FDA issued a warning letter to Avena Botanicals, Inc.

Recalls & Warnings

5/30/2020

FTC Sends Refund Checks for TrueAloe and AloeCran

On May 26, 2020, the FTC announced it is mailing 22,581 checks totaling more than $470,000 to consumers who purchased deceptively marketed supplements, TrueAloe and AloeCran.

News Release

2/14/2007

ConsumerLab.com reports on anti-depressant herb — St. John's Wort — Few supplements pass quality testing

WHITE PLAINS, NEW YORK — FEBRUARY 14, 2007 — St. John's wort may be helpful in treating mild to moderate cases of clinical depression, but a new report from ConsumerLab.com shows that few of the herbal products tested met quality standards. Americans purchased $64 million of St.

News Release

12/12/2006

Probiotic supplements grow in popularity but viable bacteria missing in many — ConsumerLab.com cautions consumers to select probiotics carefully and store them properly

WHITE PLAINS, NEW YORK — DECEMBER 12, 2006 — Sales of supplements containing beneficial organisms (probiotics) have grown rapidly, but a new test report from ConsumerLab.com shows that 44% contained fewer viable organisms than claimed or generally known to be effective.

News Release

11/13/2006

Tests of "muscle" supplements finds some "weak" products but most contain expected creatine, HMB, or amino acids — Review of muscular enhancement supplements published by ConsumerLab.com

WESTCHESTER, NEW YORK — MONDAY, NOVEMBER 13, 2006 — Bodybuilders and athletes often turn to supplements to enhance muscle size and strength.

Recalls & Warnings

3/30/2021

Real Water Alkaline Water Recalled for Possible Link to Liver Illness

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

Recalls & Warnings

5/14/2014

Maker of Mood, Smoking Cessation Supplements and More Warned for Violations, Drug Claims

On April 17, 2014, the FDA issued a warning letter to CDJ Holding, Incorporated, d.b.a.

Recalls & Warnings

4/28/2020

Natures CBD Oil Distribution Warned for Joint Pain Claims

On April 20, 2020, the FDA issued a warning letter to Homero Corp DBA Natures CBD Oil Distribution, following an inspection of the company's website which found the company's products, including Natures Pure CBD Oil, CBD Froggies 25mg, CBD Froggies 50mg, CBD Edibles 200mg Frogs, CBD ...

Recalls & Warnings

5/10/2021

Collagen & Biotin Supplement Recalled Due to Allergen Risk

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

Recalls & Warnings

8/17/2021

Love & Peas Protein Rich Meal Replacement Recalled

On July 30, 2021, Nature's Sunshine issued a recall of certain lots of Love & Peas Protein Rich Meal Replacement because it may contain milk.

Recalls & Warnings

10/13/2018

Pharmaceutical Drugs Found In Dietary Supplements Pose Danger to Consumers

Almost 800 dietary supplements sold between 2007 and 2016 contained unapproved pharmaceutical ingredients, according to a study published today in the Journal of the American Medical Association (JAMA).

News Release

10/20/2006

ConsumerLab.com report on CoQ10 supplements finds quality high but large range in suggested dosage

WHITE PLAINS, NEW YORK — OCTOBER 20, 2006 — New test results from ConsumerLab.com for CoQ10 supplements show that all of the products selected contained amounts of ingredient consistent with their labels.

News Release

11/18/2003

ConsumerLab.com reports improvement in quality of SAM-e supplements used for osteoarthritis and depression — But a high priced product found to contain only 30% of label claim

WHITE PLAINS, NY — November 18, 2003 — ConsumerLab.

News Release

9/24/2003

Consumerlab.com finds new forms of creatine prone to problems — Test results of muscular enhancement supplements published online today

WHITE PLAINS, NY — September 24, 2003 — Testing by ConsumerLab.com of creatine supplements found problems with the majority of products sold in liquid, effervescent and chewable forms. Problems were not found among standard creatine "powder" products.

News Release

8/28/2003

Some problems persist with ginseng supplements but overall quality improves according to ConsumerLab.com — Test results published online today

WHITE PLAINS, NY — August 28, 2003 — In contrast to its testing three years ago in which nearly 60% of Asian and American Ginseng supplements were found to have significant problems, testing of recently purchased products by ConsumerLab.

News Release

7/31/2003

ConsumerLab.com finds many cholesterol-lowering supplements poorly made — Test results published online today

WHITE PLAINS, NY — July 31, 2003 — ConsumerLab.com reported today that more than half of the cholesterol-lowering supplements that it recently purchased failed to contain their listed ingredients and/or could not adequately break apart to release their contents.

News Release

7/10/2002

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.

Recalls & Warnings

3/18/2021

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

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

Recalls & Warnings

11/27/2018

More Dog Food Recalled Due to Risk of Vitamin D Toxicity

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

Recalls & Warnings

11/06/2018

Dog Food Recalled After Reports of Vitamin D Toxicity

On November 2, 2018, Natural Life Pet Products and Nutrisca issued a recall of certain dry dog foods because they contain elevated levels of vitamin D. The elevated levels of vitamin D were found during an investigation into several reports of vitamin D toxicity by pet owners.

Recalls & Warnings

8/20/2019

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

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

Recalls & Warnings

12/01/2017

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

6/27/2017

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

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

Recalls & Warnings

6/06/2017

Seller of Herbal Supplements Warned for Manufacturing Violations, Drug Claims

On May 25, 2017 the FDA issued a warning letter to Life Rising Corporation, following a facility inspection which found the company's products, including Stomach Regulator, Fang Feng Formula, Skin Regulator, Regulate Liver, Circulation Regulator, Pancreas Support, Lung Regulator, Pure Tea, ...

Recalls & Warnings

6/10/2017

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

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

Recalls & Warnings

10/11/2016

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

6/23/2017

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

8/09/2002

Recall of 7 Herbal Products from Botanic Lab in US and Abroad

The U.S. Food and Drug Administration (FDA) released the following Class II recall information in its August 7, 2002 Enforcement Report.

Recalls & Warnings

11/06/2014

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

10/10/2014

Seller of Multivitamin Warned for Drug Claims

On September 25, 2014, the FDA issued a warning letter to Multimmunity, Inc., following a review of the company's website which found statements made about the dietary supplement Multimmunity to be drug claims.

Recalls & Warnings

9/26/2014

FDA Warns Seller of Supplements and Chocolate Promoted to Treat Ebola

On September 23, 2014, the FDA issued a warning letter to Natural Solutions Foundation, following a review of the company's websites which found statements made about Silver Sol Nano Silver (also called The Silver Solution) and CBD Organic Dark Chocolate Bars (also called High Potency CBD Hemp Oil) ...

Recalls & Warnings

2/05/2019

Hill's Science Diet, Prescription Diet Dog Food Recalled Due to Risk of Vitamin D Toxicity

Recall Expanded (3/20/19): This recall was expanded to include additional products.

Recalls & Warnings

6/21/2002

Canadian Warning on Use of Seven Herbal Supplements from BotanicLab

On June 19, 2002, Health Canada issued a warning that Canadians not use seven herbal products manufactured in the United States by BotanicLab because they contain undeclared prescription drugs that could cause serious health effects if not taken under medical supervision.

Recalls & Warnings

9/26/2014

Sellers of Essential Oils Warned for Claiming to Treat Ebola, Other Diseases

On September 22, 2014, the FDA issued a warning to Young Living following a review of websites, Pinterest, Facebook and Twitter accounts owned by Young Living distributors, which found statements made about the company's essential oils, including Thieves, Cinnamon Bark, Oregano, ImmuPower, ...

Recalls & Warnings

9/26/2014

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

6/13/2012

Tart Cherry Supplement Selller Warned by FDA Over Illegal Health Claims

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

Recalls & Warnings

9/05/2014

Seller of "Nerve", "Cleanse" and Probiotic Supplements Warned for Drug Claims

On July 30, 2014, the FDA issued a warning letter to Plexus Worldwide, Inc., following a review of the company's website and product labels, which found statements made about Fast Relief, BioCleanse and ProBio5 to be drug claims.

Recalls & Warnings

8/26/2014

Seller of Immune Supplement Warned for Drug Claims

On August 12, 2014, the FDA issued a warning letter to Ad-Med Biotechnology, following a review of the company's websites and product labels, which found statements made about Immune Active Adult Formula and Immune Active Children's Formula to be drug claims. 

Recalls & Warnings

9/26/2015

Seller of Muscle Supplements and More Warned for Manufacturing Violations

On August 14, 2015, the FDA issued a warning letter to Chaotic Labz, Inc.

Recalls & Warnings

9/05/2015

Maker of Multivitamin and Fish Oil Warned for Manufacturing Violations

On July 22, 2015, the FDA issued a warning letter to Westar Nutritional Corp. dba Viva Life Science, Inc.

Recalls & Warnings

5/03/2011

FDA Warns: Beware of Bogus STD Products

On May 3, 2011, the U.S. Food and Drug Administration (FDA) and the Federal Trade Commission (FTC) announced a joint effort to remove products from the market that make unproven claims to treat, cure, and prevent sexually transmitted diseases (STDs).

Recalls & Warnings

3/28/2008

FDA Warns of Adverse Reactions with Two Liquid Supplements -- Selenium Toxicity Possible

The U.S. Food and Drug Administration is advising consumers not to purchase or consume Total Body Formula in the flavors of Tropical Orange and Peach Nectar, or Total Body Mega Formula in the Orange/Tangerine flavor.

Recalls & Warnings

8/26/2014

Supplement Maker Warned for Manufacturing Violations

On August 14, 2014, the FDA issued a warning letter to dietary supplement manufacturer Big Easy Confections 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 ...

Recalls & Warnings

5/30/2017

Seller of Vitamin C, Calcium, Mushroom Supplements and More Warned for Manufacturing Violations

On May 12, 2017 the FDA issued a warning letter to VitaPurity Corporatio.

Recalls & Warnings

4/11/2008

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

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

Recalls & Warnings

1/21/2015

Supplement Maker Ordered to Stop Selling Products

On January 15, 2015, a federal judge ordered a permanent injunction against dietary supplement manufacturer Health One Pharmaceuticals, Inc. which requires the company to stop manufacturing and selling dietary supplements.

Recalls & Warnings

10/31/2014

Seller of "Cleanse," Allergy Supplements and More Warned for Manufacturing Violations, Drug Claims

On October 15, 2014, the FDA issued a warning letter to Evangelical Christian Ministries, dba Health & Herbs, following a facility inspection which found the company's products, CORYDALIS and CVF BGONE to be adulterated because they were prepared, packed, or held under conditions that violate ...

Recalls & Warnings

7/26/2014

Marketers of Nopal Cactus Drink Settle FTC Charges of Deceptive Claims

TriVita Inc., and marketers of the company's "prickly pear" fruit drink Nopalea have agreed to pay $3.5 million in consumer refunds to settle FTC charges they made deceptive claims that the drink treats health problems ranging from skin conditions to joint pain and respiratory problems.

Recalls & Warnings

1/31/2015

Maker of Soy and Zinc Warned for Manufacturing Violations

On December 18, 2014, the FDA issued a warning letter to PreMark Health Science, Inc.

Recalls & Warnings

3/10/2015

Seller of Vision Supplements Warned for Manufacturing Violations, Drug Claims

On February 26, 2015, the FDA issued a warning letter to Biosyntrx, following a facility inspection which found the company's products, including BioTears Oral Gel Caps, ZoOmega-3 Concentrated Pharmaceutical-Grade Fish Oil, EpiCor A Nutrient-dense High Metabolite Immunogen, Sight C+ Mineral ...

Recalls & Warnings

5/30/2015

Seller of Supplements for Herpes, Prostate Cancer & More Warned for Drug Claims

On May 7, 2015, the FDA issued a warning letter to Strictly Health Corporation, following a review of the company's websites which found statements made about FENVIR, Prosta Pep and Tonalin brand CLA to be drug claims.

Recalls & Warnings

12/29/2015

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

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

Recalls & Warnings

11/18/2003

Supplement Promoted As Cancer Treatment Removed from Market

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

Recalls & Warnings

9/10/2012

Maker of Omega-3, Bone and Brain and Supplements Warned For Drug Claims

On August 27, 2012, the FDA issued a warning letter to PruTect Rx indicating that statements on the company's websites about Omega3PruTect, NeuroPruTect, VitaminD3PruTect and OsteoPruTect constitute drug claims, although the products are not approved drugs.

Recalls & Warnings

6/04/2012

FDA Warning on Supplement for Pain Relief

On June 1, 2012, the U.S. FDA warned consumers that Reumofan Plus, marketed as a “natural” dietary supplement for pain relief and other serious conditions, contains several active pharmaceutical ingredients not listed on the label that could be harmful.

Recalls & Warnings

11/18/2015

Seller of "Hangover" Supplement Warned for Manufacturing Violations & Drug Claims

On September 17, 2015, the FDA issued a warning letter to Life Support Development Ltd, following a facility inspection which found the company's product, including Life Support Hangover Relief to be adulterated because they prepared, packed, or held under conditions that violate ...

Recalls & Warnings

8/23/2015

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

8/11/2015

Company Ordered to Stop Making and Selling Supplements

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

Recalls & Warnings

6/03/2015

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

5/23/2015

Seller of Magnesium, Calcium, Silver and More Warned for Manufacturing Violations, Drug Claims

On May 8, 2015, the FDA issued a warning letter to Pick and Pay, Inc.

Recalls & Warnings

2/28/2015

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

2/24/2015

Seller of Heart, Brain and Diabetes Supplements Warned for Drug Claims

On February 6, 2015, the FDA issued a warning letter to LCW, Inc.

Recalls & Warnings

1/17/2015

Supplement Maker Warned for Manufacturing Violations

On August 5, 2014, the FDA issued a warning letter to Engineering Nutrition, following a facility inspection which found the company's products, which were not named, to be adulterated because they were prepared, packed, or held under conditions that violate Current Good Manufacturing Practices for ...

Recalls & Warnings

1/17/2015

Maker of Magnesium and Potassium Supplements Warned for Manufacturing Violations

On December 23, 2014, the FDA issued a warning letter to Nutri Spec, Inc.

Recalls & Warnings

12/30/2014

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

12/30/2014

Maker of Aloe, Weight Loss Supplements and More Warned for Manufacturing Violations, Drug Claims

On December 17, 2014, the FDA issued a warning letter to Dandy Day Corporation, following a facility inspection which found the company's products, including Aloe Pearl, Alfalo, Aloespring, Crave Away, Original Supreme Energy, Ener "G," Can G, Flora G, Flora G Plus, and Garolic, to be adulterated ...

Recalls & Warnings

12/12/2014

Seller of Omega-3 "Syrup" Warned for Manufacturing Violations and Drug Claims

On October 16, 2014, the FDA issued a warning letter to Mr.

Recalls & Warnings

1/27/2015

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

On January 8, 2015, the FDA issued a warning letter to Aloe Man, Inc., following a facility inspection which found the company's products, including The Aloe Man's Super Bright, Dr. Johnson's Maximum Desire, Dr. Johnson's Body Healer, and Dr.

Recalls & Warnings

1/23/2015

Maker of Vitamin Drinks Warned for Manufacturing Violations

On January 7, 2015, the FDA issued a warning letter to NYSW Beverage Brands, Inc.

Recalls & Warnings

2/10/2015

Seller of "Natural" Cough Syrup Warned for Manufacturing Violations, Drug Claims

On January 21, 2015, the FDA issued a warning letter to Fragrance Manufacturing Incorporated, following a facility inspection which found the company's products, including Maty's All Natural Cough Syrup and Maty's All Natural Cough Syrup for Kids, to be adulterated because they ...

Recalls & Warnings

10/30/2014

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

11/11/2014

Maker of Children's Vitamins, Weight Loss Supplements and More Warned for Manufacturing Violations

On October 30, 2014, the FDA issued a warning letter to VitalHealth Tech, Inc., following a facility inspection which found the company's products, including Kids Mighty Vites tablets, Omni Jr.

Recalls & Warnings

11/11/2014

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

10/21/2014

Seller of Weight Loss Supplements Warned for Manufacturing Violations and Drug Claims

On October 7, 2014, the FDA issued a warning letter to YoungYou International, Inc.

Recalls & Warnings

10/16/2014

Seller of Black Cohosh, Ginkgo and More Warned For Manufacturing Violations and Drug Claims

On April 2, 2014, the FDA issued a warning letter to Pure Herbs, Ltd.

Recalls & Warnings

8/26/2014

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

3/28/2011

Dangerously High Levels of Vitamins A and D in Product Prompt FDA Warning

On March 28, the U.S. FDA warned consumers to stop using Soladek, a vitamin-solution product marketed by Indo Pharma, S.A., of the Dominican Republic, because the product may contain dangerously high levels of vitamins A and D.

Recalls & Warnings

12/12/2014

Seller of B-12, Zinc, Echinacea and More Warned for Manufacturing Violations and Drug Claims

On November 14, 2014, the FDA issued a warning letter to Scientific Botanicals Company, Inc.

Recalls & Warnings

10/21/2014

Seller of Weight Loss, Saw Palmetto Supplements and More Warned for Drug Claims

On October 9, 2014, the FDA issued a warning letter to Bethel Nutritional Consulting, Inc., following a review of the company's website which found statements made about 15 Day Detox Diet, Alpha Lipoic Acid. 300 mg.

Recalls & Warnings

1/03/2004

FDA to Prohibit Sales of Dietary Supplements Containing Ephedra

On December 30, 2003, the U.S. Food and Drug Administration (FDA) issued a consumer alert of its forthcoming determination that dietary supplements containing ephedra present an unreasonable risk of illness or injury, and should not be consumed.

Recalls & Warnings

10/03/2014

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

10/24/2012

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

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

Recalls & Warnings

2/24/2015

Seller of Antioxidant Water, Energy Drops Warned for Manufacturing Violations and Drug Claims

On February 18, 2015, the FDA issued a warning letter to Better Health Lab, Inc.

Recalls & Warnings

12/16/2015

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

9/11/2015

Thirteen Manufacturers Ordered to Stop Selling Devil's Claw Supplements

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

Recalls & Warnings

10/09/2013

FDA Warns Consumers Not to Use OxyElite Pro As It Investigates Link With Hepatitis

On October 8, 2013, the FDA warned consumers not to buy or use USPLabs’ weight loss supplement OxyElite Pro because it has been linked with 24 cases of acute non-viral hepatitis in Hawaii.

Recalls & Warnings

5/30/2014

Seller of Brain, Diabetes, Echinacea Supplements and More Warned for Drug Claims

On April 22, 2014, the FDA issued a warning letter to Mundo Natural Inc., following a review of the company's website which found statements made about supplements Neuro AD, Stop Diabetes, Stop High Blood Pressure, Morninga 7 and Purpurea Echinacea to be drug claims.

Recalls & Warnings

9/07/2002

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

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

Recalls & Warnings

10/05/2011

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

3/10/2015

Maker of Magnesium, Calcium, Zinc, B Vitamins and More Warned for Manufacturing Violations, Drug Claims

On January 8, 2015, the FDA issued a warning letter to Complete H2O Minerals, following a facility inspection which found the company's products, including Sulfur Concentrate, Copper, Extra Strength Copper, Extra Strength Magnesium, Extra Strength Zinc, Platinum, Gold, Indium, Molybdenum, ...

Recalls & Warnings

5/30/2015

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

10/30/2014

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

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

Recalls & Warnings

11/07/2015

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

6/11/2015

FDA Warns Maker of Fruit Energy Drinks for Drug Claims

On May 19, 2015, the FDA issued a warning letter to CK Management, Inc. following a facility inspection which found statements made on product labels and websites about Whole5, Fruit of the Spirit and ViaViente "whole food" fruit puree energy drinks to be drug claims.

Recalls & Warnings

6/26/2015

Seller of CoQ10, Anxiety Supplements and More Warned for Manufacturing Violations, Drug Claims

On June 6, 2015, the FDA issued a warning letter to Country Doctor Herbals, following a facility inspection which found the company's products, including  Herbal Flu Be-Gone, Herbal Multi-Bac, Herbal Nervine, Herbal Pain-A-Way, Herbal Pancreas, Herbal Parasite Cleanse, Herbal Perfect ...

Recalls & Warnings

8/29/2012

Herbal Supplement Company Warned For Medical Claims

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

Recalls & Warnings

5/07/2012

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

1/04/2012

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

6/21/2010

FDA Warns Parents to Be Careful Giving Vitamin D Drops to Infants

On June 15, 2010, the U.S. FDA (Food and Drug Administration) alerted parents and caregivers that some liquid Vitamin D supplement products are sold with droppers that could allow excessive dosing of Vitamin D to infants.

Recalls & Warnings

4/11/2008

Update: Hazardous Levels of Selenium Confirmed by FDA in Two Supplements

On April 11, 2008, the FDA notified healthcare professionals and patients that it has found hazardous levels of selenium in samples of certain flavors of the dietary supplement products "Total Body Formula" and "Total Body Mega Formula.

Recalls & Warnings

7/01/2003

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

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