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November 21, 2024

Umary Hyaluronic Acid Sold on Amazon Recalled

On November 20, 2024, MXBBB issued a recall of one lot of Umary Hyaluronic Acid or Amazy Hyaluronic Acid supplements, which were sold on Amazon.

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.

October 08, 2024

AK Forte Joint Pain Supplement Recalled

On October 8, 2024, C&A Naturistics voluntarily recalled all lots of AK Forte, 400 mg tablets because FDA laboratory analysis found products to contain undeclared diclofenac, dexamethasone, and methocarbamol.

December 19, 2024

Force Forever Joint Pain Supplement Recalled

On December 12, 2024, GNMart INC recalled all lots of Force Forever, a supplement promoted for joint pain, because FDA tests found it to contain undeclared diclofenac and dexamethasone.

March 16, 2023

Omega-3 Supplements for Dogs and Cats Recalled Due to Potential for Vitamin A Toxicity

On March 9, 2023, Stratford Care USA issued a recall of 62 brands of omega-3 supplements for dogs and cats due to potentially elevated levels of vitamin A.

June 16, 2022

Omega 3 Supplements Recalled Due to Undeclared Drug Ingredients

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

October 26, 2023

Joint Pain Supplements Recalled Due to Undeclared Drug Ingredients

On October 22, 2023, Botanical-Be recalled of all lots of the company’s Kuka Flex Forte, Artri King, and Reumo Flex capsule products after FDA laboratory analysis found them to contain undeclared diclofenac.

November 09, 2023

InnoMark Warned for Manufacturing & Misbranding Violations

On September 1, 2023, the FDA issued a Warning Letter to InnoMark, Inc.

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.

December 04, 2023

Manischewitz Dark Chocolate Coins Recalled Due to Undeclared Milk

On December 1, 2023, Manischewitz issued a recall of one lot of Manischewitz Dark Chocolate Coins because they contain undeclared milk. The recalled lot of coins are labeled as “dark chocolate,” but contain milk chocolate coins.

October 19, 2023

Jay Robb Protein Powder Recalled

On October 13, 2023, Select Custom Solutions recalled one lot of Jay Robb Vanilla Flavored Egg White Protein 24 oz because the product may contain hard, plastic, foreign material which could pose a choking hazard. No adverse events have been reported to date.

July 26, 2023

FDA Warns Wise Women’s Choice for Promoting Plant-Based Product for Contraception

On July 20, 2023, the FDA issued a warning letter to Wise Women’s Choice following a review of the company’s website and social media, which found statements about the company’s Wise Women’s Choice products to be drug claims because products were intended to affect ...

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.

February 22, 2024

Pacific BioLogic Co. Warned by FDA for Manufacturing Violations

On December 21, 2023, the FDA issued a Warning Letter to Curtis Jacquot, dba Pacific BioLogic Co.

July 07, 2020

All Clean Hand Sanitizer Recalled

On July 6, 2020, ITECH 361 recalled All Clean Hand Sanitizer, Moisturizer and Disinfectant because it may contain methanol, which is toxic when absorbed through the skin or ingested.

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.

August 17, 2022

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

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

March 30, 2023

Seller of Tollovid Supplements Warned for COVID-19 Claims

On November 7, 2022, the FDA issued a warning letter to Todos Medical Ltd, aka Todos Medical USA Inc, following a review of the company’s websites, social media, and Amazon storefronts, which found statements about the company’s Tollovid 3CL Protease Inhibitor Delayed Release ...

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.

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.

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.

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.

June 22, 2021

Prairie Wolf Hand Sanitizer Recalled

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

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.

January 28, 2021

FDA Issues Import Alert on Potentially-Dangerous Hand Sanitizers from Mexico

On January 26, 2021, the FDA announced that all alcohol-based hand sanitizers from Mexico will be placed on a countrywide import alert to limit the flow of potentially dangerous products into the US.

September 26, 2020

Cognitive Enhancement Supplements Can Contain Unapproved Drugs

Recent testing detected five unapproved drugs in 10 over-the-counter cognitive enhancement and workout supplements sold in the US.

March 26, 2021

Nine Banned Stimulants Found in Workout, Weight Loss Supplements

Recent analysis of 17 brands of sports/energy and weight loss supplements sold in the U.S. found nine prohibited stimulants formulated into eight different combinations, and none of these combinations have been studied in people.

June 27, 2020

Hand Sanitizer That May Contain Toxic Ingredient is Recalled

Update: (6/29/20) Saniderm has extended the recall of hand sanitzer nationwide.

August 27, 2020

Zanilast+gel Hand Sanitizer Recalled

On August 26, 2020, Nanomateriales, SA de CV recalled Zanilast+gel because it may contain 1-propanol, which is toxic when ingested.

May 05, 2022

Seller of CBD Tinctures, Creams & Pet Products Promoted for Pain, Cancer & More Warned by FDA

On February 11, 2022, the FDA issued a warning letter to Rena’s Organic following a review of the company’s social media and website, which found statements about the company’s 300 mg CBD Full Spectrum Oil Cannabinoid Tincture, 600 mg CBD Full Spectrum Oil Cannabinoid ...

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.

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.

December 24, 2020

Wash-Free Hand Sanitizer With Potentially Toxic Ingredient Recalled

On December 23, 2020, Shane Erickson, Inc.

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.

July 21, 2020

Optimus Instant Hand Sanitizer Recalled

On July 20, 2020, LIQ-E S.A. de C.V. recalled Optimus Instant Hand Sanitizer because it may contain methanol, which is toxic when absorbed through the skin or ingested.

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.

August 20, 2020

Goldenseal Recalled Due to Microbial Contamination, One Death Reported

On August 17, 2020, Maison Terre issued a recall of all lots of organic Goldenseal Root Powder because recent testing found it has the potential to be contaminated with various microorganisms including Enterobacter cloacae, Cronobacter sakazakii, Cronobacter dublinensis, and others.

March 16, 2021

Albek de Mexico Hand Sanitizer Contains Dangerous Ingredient

On March 11, 2021, the FDA issued a warning letter to Albek de Mexico S.A. de C.V. because laboratory tests showed that their product NEXT ADVANCED ANTIBACTERIAL HAND SANITIZER contains methanol, which is toxic when absorbed through the skin or ingested.

March 09, 2021

FDA Warns Sellers of Three More Hand Sanitizers, One with Toxic Ingredient

On March 1, 2021, the FDA issued warning letters to three sellers of hand sanitizers because laboratory tests showed that their products do not contain the amount of ethanol as stated on their labels. The products are MEDICALLY MINDED Hand Sanitizer Gel from Plasticos Las Palmas, S.A. de C.

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.

August 20, 2020

Yacana Hand Sanitizer Recalled

On August 18, 2020, Grupo Yacana México S.A.S De C.V. recalled Yacana Hand Sanitizer because it may contain methanol, which is toxic when absorbed through the skin or ingested. The products also may have a sub-potent ethanol content, which leads to a lack of efficacy.

July 28, 2020

FDA Warns Eskbiochem for Hand Sanitizers That May Contain Toxic Ingredient

On July 23, 2020, the FDA issued a warning letter to Eskbiochem SA de CV which found the company's products, including ClearCare Nogerm ADVANCED HAND SANITIZER and LAVAR GEL HAND SANITIZER, to be adulterated because they were prepared, packed, or held under conditions that violate ...

September 01, 2020

Harmonic Nature Hand Sanitizer Recalled

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

August 26, 2020

Asiaticon Hand Sanitizers Recalled

On August 25, 2020, Asiaticon SA de CV recalled V-Klean Hand Sanitizer Gel, Medically Minded Hand Sanitizer Gel, and Protz Real Protection Antibacterial Hand Sanitizer because they may contain methanol, which is toxic when absorbed through the skin or ingested.

August 25, 2020

Florence Morris Antiseptic Hand Sanitizer Recalled

On August 17, 2020, Grupo Asimex De Mexico Sa De CV recalled Florence Morris Antiseptic Hand Sanitizer because it may contain methanol, which is toxic when absorbed through the skin or ingested. The products also may have a sub-potent ethanol content, which leads to a lack of efficacy.

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.

November 27, 2020

Harmonic Nature Hand Sanitizer Potentially Toxic

On November 16, 2020, the FDA issued a warning letter to Harmonic Nature S. de R.L. MI. because laboratory tests showed that their product Alcohol Antiseptic 75% Topical Solution Hand Sanitizer contains 1-propanol, which is toxic when ingested.

October 06, 2020

Hand Sanitizers Marketed for Children, Packaged in Containers Resembling Food and Drink Recalled

On October 1, 2020, Ashtel Studios recalled six hand sanitizers because they are packaged in containers resembling food and drink pouches. Hand sanitizers can be toxic if ingested, and can cause lack of coordination, slowed or slurred speech, drowsiness, coma, or death.

October 03, 2020

Some "Dairy-Free" Dark Chocolate Found to Contain Undeclared Milk

On October 1, 2020, the FDA announced findings from a study it conducted from 2018 to 2019 that showed that some dark chocolate products claiming to be "dairy-free" or "milk-free" contain undeclared milk.

February 02, 2021

FDA Warns Seller of Reishi Mushroom Supplements

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

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.

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 ...

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).

May 01, 2021

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

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

April 24, 2021

Durisan Recalls Hand Sanitizer Due to Microbial Contamination

On April 10, 2021, Durisan announced a recall expansion of Durisan Antimicrobial Hand Sanitizer, NonAlcohol to include non-expired products because they may be contaminated with the bacterium Burkholderia contaminans.

December 31, 2020

Herbacil Hand Sanitizer Contains Dangerous Ingredient

On December 21, 2020, the FDA issued a warning letter to Broncolin, S.A. de C.V. because laboratory tests showed that their product HERBACIL Antiseptic Hand Sanitizer contains methanol, which is toxic when absorbed through the skin or ingested.

October 01, 2020

Cleaner Hand Sanitizer Recalled

On September 8, 2020, DMM VISSION, S.A. DE C.V. recalled five lots of Cleaner Hand Sanitizer because they may contain methanol, which is toxic when absorbed through the skin or ingested.

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.

November 27, 2020

FDA Warns Seller of Potentially Toxic Hand Sanitizer

On November 19, 2020, the FDA issued a warning letter to Liq-E S.A. De C.V. because laboratory tests showed that their product Optimus Lubricants Instant Hand Sanitizer contains methanol, which is toxic when absorbed through the skin or ingested.

September 16, 2015

Weight And Enhancement Supplement Recall Expanded

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

January 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.

December 19, 2017

Blue Pearl All Natural Enhancement Supplement Recalled

On December 13, 2017, Marmex Corp. recalled all lots of its sexual enhancement supplements Blue Pearl All Natural Male Enhancement Supplement, 500mg because they were found to contain undeclared sildenafil.

September 21, 2017

Sexual Enhancement Supplements Containing Prescription Drugs Recalled

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

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

January 04, 2007

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

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

January 20, 2006

Another Ginkgo Supplement Recalled

On January 19, 2006, Olympian Labs informed ConsumerLab.com that it recently issued a recall of a line of Ginkgo biloba supplements because the products "did not meet our specifications that our raw material supplier was contracted to follow.

June 22, 2010

Pet Vitamin Recalled for Salmonella Risk

On June 22, 2010, the FDA reported that United Pet Group, Cincinnati, Ohio is voluntarily recalling all unexpired lots of its PRO-PET ADULT DAILY VITAMIN Supplement tablets for Dogs due to possible Salmonella contamination. This product is not among those included in ConsumerLab.

August 30, 2015

Weight and Enhancement Supplements Recalled

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

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.

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. 

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.

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 ...

March 30, 2011

More Protein Supplements Recalled for Salmonella Risk

On March 29, the U.S.

October 10, 2003

Government Stops Sale of Supplements Claiming to Treat Obesity and Impotence

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

June 15, 2009

Sexual Enhancement Supplement Recalled -- Second Time Found with Drug-like Compound

On June 15, 2009, the U.S. FDA announced that, per its order, Hi-Tech Pharmaceuticals, Inc. is conducting a nationwide voluntary recall of the company's product sold under the name Stamina-Rx.

June 14, 2007

Marketers of Bogus Growth Hormone Sprays Settle with FTC

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

November 04, 2002

Recall Of Selected Store Brand Infant Formula in U.S.

On November 1, 2002, Wyeth Nutrition, in consultation with the U.S.

June 30, 2013

Weight Loss Supplements Recalled Due To Undeclared Drug

On May 21, 2013, the Dolphin Intertrade Corp. issued a voluntary recall of one lot of weight loss supplement JaDera and all lots of weight loss supplement Xiyouji Qingzhi, which were found to contain the undeclared drug sibutramine.

April 19, 2017

Sexual Enhancement Supplements for Men and Women Recalled

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

April 15, 2017

Hyland's Baby Teething Tablets and Nighttime Teething Tablets Recalled

On April 13, 2017, Standard Homeopathic Company its Hyland's Baby Teething Tablets and Hyland's Baby Nighttime Teething Tablets because FDA testing has found the tablets contain inconsistent amounts of belladonna alkaloids that may differ from the calculated amount on the ...

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 ...

October 05, 2019

Advocare to Pay $150 Million to Settle Charges of Operating a Pyramid Scheme

AdvoCare International, the marketing company that sells Spark energy drink, as well as other nutrition products and supplements, has agreed to settle FTC charges that it operated an illegal pyramid scheme.

June 02, 2020

FTC Sends Refund Checks for "ReJuvination" Supplement

On June 1, 2020, the FTC announced it is mailing 1,310 checks totaling nearly $149,000 to consumers who purchased ReJuvination, a product deceptively marketed as a cure-all for various age-related conditions, including cell damage, heart attack damage, brain damage, and deafness.

August 16, 2019

Lavender Oil Linked With Abnormal Breast Growth in Children

The use of products containing lavender oil has been linked to 16 cases of premature and/or abnormal breast development in girls and boys under the age of 8, according to a new report published in The Journal of Clinical Endocrinology & Metabolism.

January 27, 2003

FTC Charges Dr. Clark and Related Companies with Making Unsubstantiated Health Claims

The Federal Trade Commission has charged a Switzerland-based company and its U.S. counterpart with making numerous unsubstantiated efficacy claims for a variety of dietary supplements and devices that they sell on the Internet.

April 14, 2018

Men's Sexual Enhancement Supplement Recalled

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

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 ...

June 20, 2002

Canadian Warning on Use of Bejai Bowyantan for Infants

On June 14, 2002, Health Canada warned Canadians not to use Bejai Bowyantan for their young children and infants because it contains a substance with similar toxic properties to another substance known to cause serious adverse reactions and death in children.

November 27, 2011

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

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

July 15, 2011

FDA Inspection Finds Manufacturing Problems with Several Supplements Including Women's Multivitamin

The U.S. FDA recently posted a Warning Letter sent to BioSan Laboratories of Derry, New Hampshire on June 17, 2011 concerning multiple violations of Good Manufacturing Practice regulations and labeling rules.

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.

June 28, 2014

Chia Seed Recall Expanded

On June 26, 2014, HEALTH MATTERS AMERICA INC.

October 24, 2003

Court Closes the Doors on Company That Sold Weight Loss Supplement

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

August 16, 2006

Marketers of Diabetes Supplement Banned From Claiming Products Treat or Cure Diseases

On August 10, 2006, the Federal Trade Commission (FTC) announced that an operation selling Chinese herbal supplements is banned from claiming its products treat or cure diseases, to settle FTC charges it violated a previous court order.

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.

May 01, 2009

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

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

June 25, 2014

Red Yeast Rice Product Recalled

On June 24, 2014, Doctor's Best announced a voluntary recall of lot 3121005 (7379 bottles) of Red Yeast Rice dietary supplement, 600 mg Capsules, 120-count bottles.

August 02, 2013

Vitamin B, Vitamin C and Multimineral Supplements Recalled Due To Anabolic Steroid Risk

On July 31, 2013, Purity First Health Products, Inc.

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.

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.

September 01, 2011

Recall of Prenatal Supplement Due to Egg Allergen

According to the FDA website, on August 31, 2011, Pure Encapsulations announced the voluntarily recall of it "PreNatal Nutrients" supplement, lot number 3560111, because it may contain undeclared egg allergen.

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.

October 14, 2015

Recall of Male Enhancement Supplement Expanded

On October 9, 2015, TF Supplements expanded its previous recall of two lots of RHINO 7 sexual enhancement supplements, which were found to contain the undeclared drugs desmethyl carbondenafil and dapoxetine, to include all lots.

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.

September 26, 2015

Male Enhancement Supplement Containing Antidepressant Recalled

On September 25, 2015, TF Supplements issued a recall of two lots of the sexual enhancement supplement RHINO 7, which were found to contain the undeclared drugs desmethyl carbondenafil and dapoxetine.

February 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 ...

August 08, 2018

Extra Virgin Olive Oil That Isn't

Pompeian OlivExtra Original may contain less extra virgin olive oil than listed on the label, according to sources that spoke with Spain's digital newspaper El Español and as reported by The Olive Oil Times.

April 01, 2017

Weight Loss Supplement Containing Undeclared Drug Recalled

On March 28, 2017, Envy Me issued a recall of weight loss supplement LaBri's Body Health Atomic because it was found to contain undeclared sibutramine. Sibutramine, the active ingredient in the obesity drug Meridia, was removed from the U.S.

February 28, 2017

Multivitamin Recalled Due to Allergen Risk

On February 14, 2017, Licata Enterprises issued a recall of all lots of its Supreme One and Theravits 100 multiple vitamins because they contain fish liver oil but is labeled as containing "no common allergens.

December 26, 2008

Generic Manufacturer Suspends Production of All Tablets -- Including Generic Metoprolol Succinate ER

On December 23, 2008, KV Pharmaceutical advised the FDA that it voluntarily suspended all shipments of all of its FDA approved drug products in tablet form, including Metoprolol Succinate ER 100 mg and 200 mg products. [See related ConsumerLab.com Drug Investigation of Metoprolol Succinate ER.

September 23, 2005

FTC Continues Litigation Against Makers of CortiSlim and CortiStress Supplements

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

January 11, 2002

Canada Requests Recall of Certain Ephedra/Ephedrine Products

OTTAWA - January 10, 2002 - Health Canada is requesting a recall from the market of certain products containing Ephedra/ephedrine after a risk assessment concluded that these products pose a serious risk to health.

January 07, 2002

Liver Toxicity with Kava

As announced in a December 19, 2001 letter to healthcare professionals, The Food and Drug Administration (FDA) is investigating whether the use of dietary supplements containing kava (also known as kava kava or Piper methysticum) is associated with liver toxicity.

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.

November 16, 2018

Two Popular Memory Supplements Missing Some or All of Key Ingredient

Two popular Ginkgo biloba supplements marketed to improve memory do not contain the Ginkgo biloba claimed on their labels, according to tests conducted by the U.S. Government Accountability Office (GAO).

August 02, 2014

Judge Orders BioAnue To Stop Illegal Cancer and Disease Claims

On July 23, 2014, Gloria D.

August 25, 2002

Canadian Recall and Stop-Sale Order on All Kava Products

Health Canada is issuing a stop-sale order for all products containing the herb kava after a safety assessment concluded there is insufficient evidence to support their safe use. The department is also requesting the recall of these products from all levels of the market.

February 03, 2015

Major Retailers Accused of Selling Adulterated Herbal Supplements

On February 3, 2015, the New York State Attorney General announced that his office sent letters to four major retailers, GNC, Target, Walmart, and Walgreens, for allegedly selling store brand herbal supplement products in New York that either could not be verified to contain the labeled substance, ...

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.

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.

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.

January 16, 2015

CVS Sued for Eye Health Supplement Claims

A class-action lawsuit has been filed against CVS for promoting the company's Advanced Eye Health supplement as comparable to the formula used in the large National Institutes of Health (NIH) eye disease study known as AREDS2, despite the fact that it does not contain the same ingredients.

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.

April 16, 2016

Workout Supplement Containing Acacia Rigidula Recalled

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

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.

July 16, 2016

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

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

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.

March 23, 2018

PDX Aromatics Expands Recall of Kratom Products

On March 22, 2018, PDX Aromatics of Portland, Oregon DBA Kraken Kratom, Phytoextractum, and Soul Speciosa expanded their initial recall of certain kratom-containing powder products because they have the potential to be contaminated with Salmonella.  

December 01, 2017

Nutra Labs Recalls Sexual Enhancement Supplements Containing Undeclared Drugs

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

October 31, 2017

Black Licorice Can Cause Abnormal Heart Rhythms, FDA Warns

On October 30, 2017, the FDA warned consumers that eating 2 ounces of black licorice a day for at least two weeks could cause an irregular heart rhythm or arrhythmia in adults age 40 or older. 

July 22, 2013

Sexual Enhancement Supplements Containing Undeclared Drugs Recalled

On July 18, 2013, Volcano Company issued a voluntary recall all lots of Volcano Male Enhancement Liquid and Volcano Male Enhancement Capsules because they were found to contain undeclared desmethyl carbodenafil, dimethylsildenafil, and dapoxetine.

July 01, 2013

Teas Recalled Due To Potential Botulism Contamination

One June 28, 2013, Harmony Chai issued a voluntary recall of its Concentrated Black Spiced Chai and Decaffeinated Rooibos Chai bottled tea drinks, because they have the potential to be contaminated with Clostridium botulinum.

November 30, 2013

"Diuretic" Weight Loss Supplement Recalled

On November 29, 2013, IQ Formulations issued a recall of all lots of diuretic weight loss supplement HYDRAVAX because one lot of the supplement was found to contain an undeclared prescription diuretic drug.

February 01, 2013

DMAA Supplement Linked to Runner's Death

The cause of death of London marathon runner Claire Squires has been ruled by the investigating coroner as cardiac failure due to extreme exertion, complicated by DMAA toxicity.

April 11, 2013

Chinese Herbal Manufacturer Warned For CGMP Violations

On March 20, 2013, the FDA issued a warning letter to Finemost Corporation, dba Qualiherb, following a facility inspection which found the company's supplements, including Yi Zhi Tang and C.

June 18, 2011

FTC Attacks Massive Online Fraud Regarding "Free Trials" of Supplements and Health Products

On May 17, 2011, the U.S. Federal Trade Commission (FTC) announced that it is suing the operators of an online operation that collected more than $450 million from consumers in the United States, Canada, the United Kingdom, Australia, and New Zealand. According to the FTC's complaint:

November 03, 2011

Hoodia Marketers Fined and Banned from Business

On November 3, 2011, the Federal Trade Commission (FTC) announced that it settled charges brought against three people and two companies for deceptively advertising a supposed weight-loss supplement ingredient -- hoodia.

June 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.

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.

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.

September 15, 2010

Recall of Testosterone-Boosting Supplement

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

January 16, 2010

Recall of Body Building Supplements Containing Steroids

On January 15, 2010, the Food and Drug Administration (FDA) posted a voluntary recall notice from MuscleMaster.com, Inc. regarding all lots and expiration dates of seventeen dietary supplements sold in 2009 from June 1 and Novemember 17.

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.

February 15, 2006

New Zealand Warns of Liver Toxicity from Black Cohosh

On February 9, 2006, New Zealand's Therapeutic Goods Administration (TGA) announced new labelling and consumer information for medicines containing Black cohosh (Cimicifuga racemosa).

October 30, 2008

Possible Risk Rather than Benefit Found in Trial of Vitamin E and Selenium for Prostate Cancer

On October 27, 2008 the National Cancer Institute (NCI) announced that men in the Selenium and Vitamin E Cancer Prevention Trial (SELECT) are being told to stop taking their supplements.

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.

June 19, 2008

FDA Warns Groups to Stop Selling Fake Cancer 'Cures'

On June 17, 2008, the FDA reported that it had sent Warning Letters to 23 U.S. companies and two foreign individuals marketing a wide range of products fraudulently claiming to prevent and cure cancer.

May 29, 2008

Recall of Virility Supplement

On May 29, 2008, the FDA posted a recall by International Pharmaceuticals, Ltd. of all of the company's supplement sold under the name of Viril-Ity-Power (VIP) Tabs, 560mg/serving.

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.

July 23, 2009

Weight Loss Supplements Found to Contain Prescription Drug

On July 15, 2009, the U.S. FDA announced that Young You Corporation was recalling four weight loss supplements that contain an undeclared drug ingredient.

March 08, 2007

FTC Files Against Maker of Calcium and Fertility Supplements

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

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.

September 15, 2005

Weight Loss Pill Marketer in Settlement with New Jersey Attorney General

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

May 28, 2003

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

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

February 07, 2011

Maker of Hoodia and Green Tea Products to Pay $2.65 Million Settlement for Unfair Business Practices

On February 1, 2011, supplement maker Irwin Naturals agreed to pay civil penalties, consumer restitution, and and investigative costs to settle a suit in California alleging that Irwin Naturals marketed Hoodia products that did not contain the hoodia gordonii herb despite the product labeling.

June 02, 2016

Clif Bars Recalled Due to Listeria Risk

On June 2, 2016, Clif Bar & Company issued a recall of certain energy and trail mix bars because they contain sunflower kernels which have the potential to be contaminated with Listeria monocytogenes. 

October 17, 2015

23,000 ER Visits Linked to Supplements: Palpitations, Swallowing Problems, Allergies Common

Approximately 23,000 emergency room visits per year are attributed to adverse events linked to the use dietary supplements, according to a large, long-term study by the FDA and the Centers for Disease Control and Prevention (CDC).

July 15, 2004

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

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

January 18, 2003

Non-Prescription Anti-Hypertension Pills Recalled

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

August 28, 2018

King Bio Homeopathic Product Recall Expanded

On August 27, 2018, King Bio expanded its initial recalls of certain homeopathic products and children's homeopathic products to include all of its aqueous-based products for human and animal use due to possible microbial contamination.

May 28, 2008

FDA Requests Recall of Xiadafil VIP Supplements

On May 27, 2008, the U.S. The U.S. Food and Drug Administration announced that it had requested that SEI Pharmaceuticals, of Miami, Fla.

April 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.).

March 25, 2008

FDA Warns of Sexual Supplements with Drug-like Ingredients

On March 25, 2008, the U.S. Food and Drug Administration advised consumers not to purchase or use "Blue Steel" or "Hero" products marketed as dietary supplements throughout the United States because they are considered unapproved drugs and have not been proven to be safe or effective.

September 08, 2018

Homeopathic Oral Sprays Recalled Due to Possible Bacterial Contamination

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

February 22, 2018

Kratom Supplements Recalled and Destroyed

On February 21, 2018, the FDA announced the voluntary destruction and recall of Botany Bay, Enhance Your Life and Divinity kratom supplements. All of the products were manufactured and distributed nationwide by Divinity Products Distribution, located in Grain Valley, Missouri.

June 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 ...

March 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.

September 12, 2018

FDA Urges Consumers to Avoid Kratom

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

September 19, 2012

FDA Reports Arsenic in Rice Products -- Particularly Brown Rice

On September 19, 2012, the U.S. FDA released results of its testing of nearly 200 samples of rice and rice products, finding appreciable levels in many products, although the amounts in only a few exceed the cancer-warning threshold of the State of California (10 mcg per daily serving).

June 05, 2012

Many "Grapefruit Seed Extracts" Adulterated

On June 4, 2012, the American Botanical Council (ABC) announced the publication of a review of scientific literature regarding “grapefruit seed extracts,” raising concerns about apparent adulteration of products in the US and international marketplaces.

April 29, 2010

Vitamin D Overload in Supplement Sickens Users

On April 28, 2010, the New York Post reported that Gary Null, a nutrition promoter, was apparently sickened by his own product, Gary Null's Ultimate Power Meal, due to a manufacturing error that caused an excessive amount of vitamin D to occur in the product.

May 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).

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.

September 25, 2007

Recall of Contaminated Baby Supplement

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

May 10, 2007

FDA Warns of Two Supplements Containing Pharmaceutical-like Compounds

On May 10, 2007, the FDA advised consumers not to purchase or use "True Man" or "Energy Max" products promoted and sold as dietary supplements throughout the United States.

January 29, 2004

U.S. Action on Mad Cow -- Supplements Included As Well as Food

On Jan. 26, 2004, the U.

March 31, 2005

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

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