Reviews and Information for ON

March 12, 2016

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

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

January 04, 2024

Toxic Herb Found in More Tejocote Root Supplements

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

September 01, 2022

Elite One Source Nutritional Services Warned for Manufacturing, Labeling Violations

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

September 21, 2023

Moor Herbs, Inc Warned for Manufacturing Violations, Drug Claims

On August 1, 2023, the FDA issued a Warning Letter to Moor Herbs, Inc.

July 26, 2023

Gadget Island, Inc. Male Enhancement Supplements Found to Contain Prescription Drugs

On July 21, 2023, the FDA issued a warning letter to Gadget Island, Inc.

December 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.

May 04, 2023

FDA Warns MedoLife for Promoting Homeopathic Products to Treat COVID-19, Cancer

On April 19, 2023, the FDA issued a warning letter to Medolife Rx D/B/A MedoLife Corp., AELIA Inc. and Queanta Inc.

September 10, 2021

FDA Warns Ten Sellers of "Diabetes" Supplements

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

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.

September 14, 2023

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

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

January 03, 2024

FDA Warns Amazon for Selling Men’s Supplements Containing Prescription Drugs

On December 20, 2023, the FDA issued a Warning Letter to Amazon.com, Inc.

July 25, 2024

West Coast Laboratories Warned for Manufacturing, Labeling Violations

On March 12, 2024, the FDA issued a Warning Letter to West Coast Laboratories, Inc.

April 17, 2021

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

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

November 09, 2023

InnoMark Warned for Manufacturing & Misbranding Violations

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

September 06, 2023

WEFUN Capsules Recalled Due to Undeclared Sildenafil

On August 25, 2023, WEFUN Inc. issued a recall of 300 boxes of WEFUN Capsules after FDA analysis found the product to contain undeclared sildenafil, a prescription medication.

January 19, 2023

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

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

January 26, 2023

FDA Warns Seller of Canary Seed Omega-3

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

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 17, 2023

Seller of Ashwagandha, Lion’s Mane & Other Supplements Warned for Manufacturing Violations

On March 17, 2023, the FDA issued a warning letter to Brand Packaging Group, Inc. after FDA inspection of the company’s facility found products to be adulterated because they were prepared, packed, or held under conditions that do not meet Current Good Manufacturing Practices (CGMP).

July 19, 2023

FDA Warns Seller of Sleepy Time Products and Honey Herbal Syrups for Manufacturing Violations

On June 28, 2023, the FDA issued a warning letter to Eden’s Answers, Inc. after an inspection of the company’s facility found products to be adulterated because they were prepared, packed, or held under conditions that do not meet Current Good Manufacturing Practices (CGMP).

June 19, 2023

A&Z Pharmaceutical Warned for Promoting Calcium & Vitamin D for Hair Loss, Osteoporosis & Cancer

On June 1, 2023, the FDA issued a warning letter to A&Z Pharmaceutical, Inc. following inspection of the company’s website and social media, which found statements about the company’s Chewable Calcium 600MG with Vitamin D for Kids in Orange Flavor products to be drug claims.

October 06, 2005

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

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

May 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.

September 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.

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 ...

March 20, 2020

Seller of Rejuvenation Pills Settles Charges of Making False Claims

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

July 25, 2022

Nature’s Sunshine Protein Powder Recalled

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

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.

June 13, 2022

Homeopathic Nasal Spray SnoreStop Recalled Due to Microbial Contamination

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

July 14, 2022

FDA Warns Seller of Unauthorized COVID-19 Tests

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

April 25, 2022

Some OTC Skin Lighteners Contain Potentially Harmful Ingredient, Warns FDA

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

May 09, 2022

Natural Organics Keto Capsules Recalled Due to Gluten

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

August 16, 2023

FDA Warns Sun Ten Laboratories for Manufacturing Violations, Drug Claims

On April 7, 2023, the FDA issued a warning letter to STPCA Inc. dba Sun Ten Laboratories because products were found to be adulterated because they were prepared, packed, or held under conditions that do not meet Current Good Manufacturing Practices (CGMP).

April 27, 2023

Seller of Magtein, Veggie Caps, & More Warned for Drug Claims, Manufacturing Violations

On March 8, 2023, the FDA issued a warning letter to Spartan Enterprises Inc., dba Watershed Wellness Center, after a review of the company’s website found statements about its Dr. Bob’s Naturals Spirulina, Dr. Bob’s Naturals Magtein, Dr.

April 23, 2021

FDA Warns 5 Sellers of Unapproved COVID-19 Tests

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

March 14, 2011

22 Brands of Whey Protein Recalled Due to Salmonella Concern

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

January 04, 2024

Lone Star Botanicals Warned by FDA for Manufacturing Violations

On November 26, 2023, the FDA issued a Warning Letter to Lone Star Botanicals, Inc.

April 09, 2003

Recall of Dangerous Sexual Enhancement Supplement Illegally Containing Viagra Ingredient

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

June 02, 2022

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

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

March 09, 2022

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

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

August 15, 2020

FTC Warns 20 More Companies for Coronavirus Claims

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

June 10, 2024

StellaLife Homeopathic Oral Rinse & Spray Recalled Due to Yeast, Mold, and Bacteria

On June 5, 2024, HomeoCare Laboratories, Inc.

March 11, 2024

Healthex Warned for Manufacturing Violations

On June 15, 2023, the FDA issued a Warning Letter to Healthex Distributors, Inc.

July 16, 2024

Infla-650 Herbal Dietary Supplement Recalled

On July 16, 2024, Guru Inc. issued a recall of one lot of Infla-650 Herbal Dietary Capsules because they were found to contain acetaminophen, diclofenac, and phenylbutazone.

December 10, 2024

Aroma Vita Hot Cocoa Mix Recalled Due to Metal Fragments

On October 2, 2024, Dyma Brands Inc. issued a recall of two lots of Aroma Vita Hot Cocoa Mix, because they may contain metal fragments which, in severe cases, could lead to damage of the digestive tract if ingested.

December 19, 2024

Jarritos Coconut Water Recalled

On November 4, 2024, Tipp Distributors, Inc. issued a recall all lot codes of Jarritos Coconut Water (17.5 fl oz cans) because the airtight seal on the lid of the cans may be compromised.

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.

October 15, 2012

Recall of Nutrition Bars Containing Peanut Butter Due To Salmonella Risk

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

April 25, 2017

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

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

December 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.

May 19, 2020

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

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

December 14, 2023

FDA Warns Seller of Novid NASAL SPRAY for Allergy, Virus, and Cold Claims

On December 7, 2023, the FDA issued a warning to Novid Group, Inc. following an inspection of the company’s website, which found statements about the company’s novid NASAL SPRAY product to be drug claims.

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.

October 02, 2023

Dangerous Ingredients Found in Ten Arthritis and Pain Supplements

On September 29, 2023, the FDA warned consumers that the following arthritis and pain management products contain undeclared drugs such as diclofenac, methocarbamol (a muscle relaxant), and dexamethasone (a corticosteroid), and/or other potentially harmful ingredients.

July 26, 2023

Five Leaf Pet Botanicals Warned by FDA for Drug Claims

On June 22, 2023, the FDA issued a warning letter to Five Leaf Pet Botanicals, Inc.

June 14, 2023

Havasu Beet Root Powder Recalled Due to Allergen Risk

On June 12, 2023, Supplement Manufacturing Partner Inc. issued a recall of one lot of Havasu Nutrition’s Beet Root Powder + due to undeclared milk. The recall was initiated following a report of an allergic reaction from a consumer with a milk allergy.

May 04, 2023

PrimeZEN Enhancement Supplement for Men Found to Contain Prescription Drug

On April 27, 2023, the FDA issued a warning letter to Tager Online, Inc. DBA Volt Candy; Volt Candy Wholesale Club after FDA laboratory analysis determined PrimeZEN Black 6000, a product promoted to improve sexual function for men, contains tadalafil and sildenafil.

April 03, 2023

SimplyProtein Bars Recalled Due to Undeclared Cashews

On March 31, 2023, Wellness Natural USA Inc. issued a voluntary recall of a single lot of SimplyProtein Peanut Butter Chocolate Crispy Bars because they contain undeclared trace of tree nuts (cashews).

April 24, 2023

Terry Naturally and EuroMedica B Vitamins Recalled Due to Allergen Risk

On April 21, 2023, EuroPharma, Inc. issued a voluntary recall of 4 lots of its Terry Naturally BioActive Vitamin B 60 count and 3 lots of its EuroMedica Active B Complex 60 count products due to undeclared milk. No illnesses have been reported to date.

March 23, 2023

FDA Warns Herbal Vitality for Promoting Supplements to Treat Cold & Flu, Kidney Stones & More

On March 7, 2023, the FDA issued a warning letter to Herbal Vitality, Inc.

May 29, 2021

FDA, FTC Warns Five Sellers of "Infertility" Supplements

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

March 05, 2021

FTC Takes Further Action Against Deceptive CBD Claims

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

August 01, 2022

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

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

May 08, 2024

Razer, Inc. to Pay Over $1.1 Million Settlement for Zephyr Face Mask ”N-95” Claims

On April 29, 2024, the FTC announced it will be returning over $1.1 million to consumers who purchased Zephyr face masks after the company promoted its Zephyr face masks as N95-grade despite never submitting for testing to the FDA for approval of such claim.

February 01, 2018

Seller of Supplements for Opiate Withdrawal Warned for Drug Claims

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

August 25, 2022

Oregon’s Wild Harvest Warned by FDA for Manufacturing Violations

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

November 21, 2022

Healthy Sense and People’s Choice Multis Recalled

On November 17, 2022, Mason Vitamins Inc.

December 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.

June 08, 2022

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

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

January 19, 2022

FDA Warns Seller of Carnitine and Alpha Lipoic Acid Supplements

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

January 12, 2022

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

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

January 03, 2022

Seller of Wormwood, Aloe Supplement Warned by FDA

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

February 10, 2022

Three Sexual Enhancement Supplements Sold on Amazon Recalled

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

June 02, 2022

Prune & Senna Softgels Recalled Due to Undeclared Peanuts

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

January 18, 2002

Recall of Pepsin-containing Digestive Supplements

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

June 04, 2004

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

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

February 29, 2008

FTC Sues Sellers of Weight-Loss Pills for False Advertising

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

November 26, 2019

FDA Warns Companies Selling CBD Products as Dietary Supplements

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

April 16, 2019

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

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

May 09, 2020

FTC Warns 45 More Companies for Coronavirus Claims

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

May 23, 2020

FTC Warns 50 More Companies for Coronavirus Claims

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

February 24, 2023

Bountiful Charged with “Review Hijacking,” False Advertising of Nature’s Bounty Supplements on Amazon

On February 16, 2023, the Federal Trade Commission (FTC) charged The Bountiful Company (formerly NBTY), whose brands include Nature’s Bounty and Sundown, with deceptively using Amazon reviews and badges (such as “#1 Best Seller” and “Amazon’s Choice”) from its ...

July 12, 2023

FDA Warns Company for Promoting Kratom Products for Pain, Mood, and More

On July 3, 2023, the FDA issued a warning letter to Sunshine Trading Company, Inc.

May 08, 2024

APG SEVEN Warned for Promoting Products for Cancer, Depression, Arthritis, & More

On April 18, 2024, the FDA issued a Warning Letter to APG SEVEN, INC following a review of the company’s product labels, website, and social media, which found statements about the company’s BioMoringa, BioDiabetin, Maca Plus, BioProstate, Immune Support, HongoTrap, Honbacterol, ...

May 14, 2021

Maker of Care by Design CBD Settles Charges of Unsupported Claims

On May 5, 2021, Cannacraft, Inc.

May 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.

May 08, 2021

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

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

November 24, 2021

FDA Warns Sanitizer Corporation For Manufacturing and Misbranding Violations

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

July 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.

June 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.

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.

March 16, 2021

FDA Warns Seller of Essential Oils

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

March 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.

February 22, 2021

FDA Warns Sellers of St. John's Wort

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

February 16, 2021

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

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

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 ...

January 31, 2021

Protein and Fiber Bars Recalled Due to Allergen Risk

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

January 20, 2021

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

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

January 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.

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.

July 22, 2022

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

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

April 06, 2022

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

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

May 09, 2022

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

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

May 11, 2022

FDA Warns 10 Companies for Selling Workout Supplements With Dangerous Ingredients

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

April 23, 2019

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

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

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.

October 12, 2005

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

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

April 19, 2007

Recall of Another Sex Enhancement Supplement

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

August 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.

December 17, 2004

FDA Seizes Ginseng Because of Potentially Risky Pesticide Residues

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

July 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.

November 15, 2009

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

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

September 11, 2020

Seller of "COVID PACK" Warned for Coronavirus Claims

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

September 08, 2020

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

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

September 08, 2020

FDA Warns Seller of Multivitamin for Manufacturing Violations

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

August 13, 2020

FDA Warns Three More Companies Selling Unapproved COVID-19 Tests

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

June 30, 2020

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

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

November 10, 2020

FDA Warns Seller of Digestive Enzymes, Nattokinase, and More

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

November 02, 2020

Silver Cannot Be Promoted to Prevent or Treat COVID-19

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

October 15, 2020

FDA Warns Five Sellers of Dangerous Cesium Salt Supplements

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

June 16, 2020

FDA Warns Four Companies for Unsafe "Homeopathic" Injectables

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

June 09, 2020

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

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

January 23, 2020

Massive Recall of Supplements Sold by Over 800 Brands

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

December 24, 2020

Wash-Free Hand Sanitizer With Potentially Toxic Ingredient Recalled

On December 23, 2020, Shane Erickson, Inc.

April 21, 2011

FTC Targets Fake News Sites Making Deceptive Acai Claims

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

July 05, 2012

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

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

August 02, 2012

FDA Warns Two Supplement Makers of Manufacturing Violations

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

January 10, 2013

FDA Warns Aloe and Herbal Supplement Companies For Manufacturing Violations

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

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 19, 2004

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

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

April 01, 2004

Aloe Producer Recalls Product Due to Toxic Levels of Vitamin D

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

October 18, 2005

FTC Stops False Claims about HGH Oral Spray

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

August 31, 2009

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

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

January 02, 2012

FDA Warns XYMOGEN of Manufacturing and Labeling Violations Regarding Multiple Products

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

October 06, 2011

Testosterone Booster Supplement Recalled for Containing Synthetic Steroid

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

October 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.

February 19, 2019

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

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

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.

October 06, 2020

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

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

October 10, 2024

Seaweed Recalled Due to Allergen Risk

On October 10, 2024, Wismettac Asian Foods, Inc. recalled its 3.52 oz packages of Shirakiku Korean Seasoned Seaweed.

May 09, 2024

DaVinci Laboratories Memory Supplement Recalled

On May 8, 2024, DaVinci Laboratories issued a recall of one lot (approximately 72 bottles) of Amyloid Complete capsules because they may contain undeclared shellfish (shrimp and crab).

June 13, 2024

Thyroid Supplement Recalled Due to Salmonella

On June 11, 2024, Penn Herb Company Ltd issued a recall of 51 bottles of Nature’s Wonderland Thyroid Formula capsules after FDA testing revealed the products to be contaminated with Salmonella.

April 25, 2024

Yogi Tea Recalled Due to Pesticides

On April 19, 2024, Yogi Tea issued a recall of over 54,800 packs of Yogi Echinacea Immune Support tea after a sample of echinacea tested above acceptable limits for multiple pesticides. No illnesses have been reported to date.

April 29, 2024

Longreen Reishi and Xlim Express Coffee Recalled Due to Undeclared Allergens

On April 18, 2024, BF Suma Pharmaceuticals, Inc.

April 17, 2015

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

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

May 20, 2014

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

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

January 09, 2014

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

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

October 17, 2013

Turmeric Spice Powder Recalled Due To High Lead Levels

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

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.

August 25, 2023

FDA Warns Consumers Not to Use Big Guys Male Energy Supplement

On August 22, 2023, the FDA warned consumers not to buy or use BIG GUYS Male Energy Supplement after FDA laboratory analysis found it to contain undeclared sildenafil.

May 08, 2023

SD Biosensor Pilot At-Home COVID-19 Tests Recalled Due to Bacterial Contamination

On May 4, 2023, the FDA warned consumers and health care providers not to use certain lots of Roche Diagnostics’ SD Biosensor, Inc. Pilot COVID-19 At-Home Tests due to bacterial contamination in the test kit’s liquid solution.

January 12, 2023

FDA Warns Two Sellers Promoting CBD to Treat COVID-19

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

March 31, 2018

Supplement Manufacturer Shut Down for Manufacturing Violations

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

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.

December 05, 2015

FDA Warns Companies Selling Products Containing Picamilon

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

January 19, 2002

Recall of Certain Iron Supplements

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

June 20, 2003

FTC Charges Marketers of Seasilver with False and Deceptive Claims

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

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.

October 05, 2011

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

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

September 08, 2011

FDA Warns Several Supplement Manufacturers Not Following Good Manufacturing Practices

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

June 01, 2012

Homeopathic Manufacturer Settles False Advertising Suit

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

September 13, 2010

Supplement for "Increasing Desire" Recalled for Containing Drug

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

July 20, 2010

Recall of ED Supplement Containing Drug

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

October 05, 2007

FTC Charges Progesterone Cream Sellers with Making Unsubstantiated Claims

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

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.

August 09, 2007

FDA Warning on Red Yeast Rice Products

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

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.

April 26, 2015

FDA Identifies More Products Listing Synthetic Amphetamine

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

December 27, 2012

Two Supplement Companies Warned For Manufacturing Violations

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

November 08, 2012

Chinese Herb Recalled Due To Undeclared Sulfites

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

July 13, 2012

Alistrol Health Inc. Warned Over Health Claims on Products

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

August 24, 2012

Protein Shots, Drinks and Gelatin Recalled For Potential Botulism Contamination

On August 17, 2012, Protica Inc.

June 23, 2020

BioPure Healing Products Warned for Manufacturing Violations

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

July 31, 2020

FDA Warns Seven Sellers of "Hangover Cures"

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

August 14, 2020

The Green Herb and New Genesis Health Warned for Manufacturing Violations

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

July 07, 2020

Seller of Homeopathic Products Warned for Manufacturing Violations

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

March 05, 2020

Protein Powder Recalled Due to Undeclared Milk

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

July 01, 2022

Male Enhancement Supplements Sold on Amazon Recalled

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

July 28, 2022

FDA Warns Three Manufacturers of Sanitizer for Manufacturing and Misbranding Violations

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

July 21, 2022

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

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

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.

November 28, 2022

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

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

November 21, 2022

6 Supplement Companies Warned by FDA for Making Cholesterol Claims

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

March 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).

April 05, 2022

Sexual Enhancement Capsules for Men Recalled

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

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.

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.

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.

January 13, 2019

Sexual Enhancement Supplement Recalled

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

March 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).

November 05, 2021

Herb Recalled Due to Risk of Lead, Cadmium Contamination

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

May 04, 2021

CytoSport's Evolve Protein Shakes Recalled

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

December 01, 2021

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

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

November 23, 2022

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

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

September 05, 2015

Powdered Caffeine Risky, FDA Warns

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

January 31, 2017

Vegetarian Protein Drink Recalled Due to Undeclared Milk

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

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.

May 29, 2003

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

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

July 13, 2005

Recall of Multivitamins with Iron Lacking Child-Resistant Caps

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

March 20, 2007

Recall of Adulterated Sexual Enhancement Supplement

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

July 24, 2006

Marketers of Seasilver Ordered to Pay Almost $120 Million

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

November 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.

April 22, 2008

Court Upholds Order for Seasilver Marketers to Pay $120 Million

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

March 06, 2009

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

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

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."

December 20, 2011

Organic Celery Seed Products Recalled Due to Potential Salmonella Contamination

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

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.

December 26, 2010

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

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

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 02, 2013

FDA Finds Manufacturing Violations At NSF-Certified Supplement Facility

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

February 06, 2013

Ingredient Supplier Warned For Meal Replacement Product Misbranding and Adulteration

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

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:

April 11, 2015

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

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

January 04, 2014

Beware of Supplements Claiming to Treat Brain Injury, FDA Warns

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

December 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.

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.

July 31, 2020

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

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

July 17, 2020

Two More Hand Sanitizers That May Contain Toxic Ingredient Recalled

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

July 10, 2020

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

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

June 23, 2020

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

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

June 25, 2020

"Anti-Viral" Supplement Recalled for Unsupported Coronavirus Claims

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

December 11, 2020

Goldenseal Recalled Due to Microbial Contamination

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

February 26, 2020

Company Failed to Report Adverse Events Associated With Its Nutrition Shakes

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

February 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)).

January 24, 2020

Fat-Burning, Energy Supplement Linked to Heart Trouble

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

March 31, 2020

Bulletproof Warned for Manufacturing Violations

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

March 24, 2020

Mislabeled Lindt Chocolate Bar Recalled

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

March 09, 2020

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

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

May 09, 2020

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

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

May 12, 2020

Plum Dragon Herbs Warned for Coronavirus Claims

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

April 24, 2021

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

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

March 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.

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:

April 04, 2013

Three More Sexual Enhancement Supplements Found To Contain Undeclared Drugs

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

March 29, 2013

Prescription Drugs Found In Prostate and Sexual Enhancement Supplements

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

August 01, 2013

Fat Loss and Muscle Enhancement Supplements Found To Contain DMAA

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

October 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.

December 21, 2012

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

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

June 21, 2011

FDA Seizes Probiotics Over Marketing Claims

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

October 26, 2011

FDA Warns Supplement Maker of Manufacturing Violations Affecting Many Products

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

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.

July 15, 2010

Supplement Company Pays $5.5 Million to Settle False Advertising Claims

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

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.

October 06, 2004

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

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

March 02, 2005

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

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

February 27, 2018

Testosterone, Thyroid, Other Supplements Recalled Due to Undeclared Milk

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

May 12, 2018

Seller of Maca Powder Warned for Drug Claims

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

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.

September 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.

September 25, 2018

FDA Warns Seller of Digestive Enzyme Supplements

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

July 06, 2018

Prescript-Assist Probiotic Recall Expanded

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

June 29, 2018

Prescript-Assist Probiotic Recalled

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

November 29, 2019

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

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

October 08, 2019

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

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

October 01, 2019

Lead and Arsenic Found in Multi Mineral & Vitamin Supplement

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

September 21, 2019

Liquid Vitamin C for Men Recalled

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

April 02, 2019

FDA Issues Strong Warnings to Sellers of CBD

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

March 26, 2019

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

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

March 23, 2019

BLUEFUSION Capsules for Sexual Enhancement Recalled

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

July 23, 2019

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

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

July 16, 2019

FDA Warns Seller of Magnesium and CBD

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

June 16, 2019

"Immune Support" Throat Sprays Recalled

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

May 25, 2019

Department of Justice Files Complaint to Shut Down Supplement Company

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

June 04, 2020

FTC Warns 35 More Companies for Coronavirus Claims

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

January 23, 2020

Flaxseed Salmonella Risk Prompts Recall

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

March 17, 2004

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

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

March 09, 2004

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

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

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.

January 17, 2006

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

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

August 14, 2008

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

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

August 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.

June 18, 2016

Antioxidant Supplement Recalled Due to Allergen Risk

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

May 23, 2016

Amino Acid Supplements Recalled

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

March 08, 2016

Maker of Calcium and Vitamin C Supplements Warned for Manufacturing Violations

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

July 11, 2017

Gluten Free Chocolate Chip Bars Recalled Due to Allergen Risk

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

July 04, 2017

FDA Warns Against Company's Unsafe Teething Tablets

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

October 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.

September 23, 2017

Enhancement Supplement "Vegetable Vigra" Recalled

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

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

July 18, 2017

Oat Cereal Recalled Due to Listeria Risk

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

November 22, 2017

FDA Warns Distributor of "Testosterone Wellness for Men"

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

November 02, 2008

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

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

July 23, 2009

Six Male Enhancement Supplements Found Adulterated

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

October 07, 2011

Recall of Whey Protein Powders Due to Allergens

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

March 03, 2012

FDA Warns Vitaganic of Manufacturing Violations

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

May 13, 2012

Caffeinated Water Illegally Promoted According to FDA

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

June 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: 

April 04, 2012

Maker of Protein Drinks and Supplements Warned of Manufacturing Violations

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

March 14, 2012

Manufacturing Violations by Maker of Lecithin, Soy Supplements

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

March 07, 2012

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

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

January 31, 2012

FTC Stops Fake News Sites About Acai Berry Products

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

April 07, 2011

Prostate Drug Found in Prostate Supplement -- Recall Underway

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

August 18, 2006

Restitution Program for Purchases of Lane Labs' Products

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

June 09, 2005

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

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

January 18, 2003

Non-Prescription Anti-Hypertension Pills Recalled

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

December 11, 2002

Recall of Calcium Supplement Possibly Contaminated with Antibiotic

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

April 15, 2003

FTC Requires Scientific Evidence for "Snore Formula" Claims

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

March 04, 2003

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

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

June 30, 2002

Recall of Dalyvite Liquid Multivitamin

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

February 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.

January 16, 2013

Nutrition Bars Recalled Due To Undeclared Allergen

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

November 14, 2012

Mushroom Supplement Manufacturer Warned For Drug Claims and Adulteration

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

December 05, 2012

Hydroxycut Class Action Lawsuit To Be Settled

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

November 28, 2012

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

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

October 17, 2012

Maker of Probiotic Supplement Warned for Manufacturing Violations

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

September 10, 2012

Maker of Concussion Recovery Supplement Warned For Making Drug Claims

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

September 08, 2012

Medifast Settles False Advertising Suit

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

May 03, 2013

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

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

April 19, 2013

Recall: Contaminated Iron Supplement

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

June 12, 2013

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

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

February 04, 2013

Protein Supplement Recalled Due To Undeclared Soy and Milk

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

February 15, 2013

Energy Drink Recalled Due To Bacterial Contamination

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

February 14, 2013

Protein Drink Recalled Due To Bacterial Contamination

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

July 15, 2014

Pinnacle Labs International Warned for Manufacturing Violations

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

July 15, 2014

Vita Springs Health Warned for Manufacturing Violations and Drug Claims

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

April 03, 2014

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

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

March 21, 2014

Homeopathic Products Recalled Due to Allergy Risk

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

March 19, 2014

Maker of Herbal Capsules and Extracts Warned for Manufacturing Violations

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

August 28, 2013

Maker of Sexual Enhancement Supplement Warned for Manufacturing Violations

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

October 25, 2013

Supplement Company Warned For Numerous Manufacturing Violations

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

December 05, 2014

Maker of Immune Supplement Warned for Manufacturing Violations

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

July 01, 2014

Maker of Elderberry Concentrate Warned for Manufacturing Violations

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

June 19, 2018

FDA Warns Seller of Weight Control Patches

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

June 05, 2018

FDA Warns Seller of Colloidal Silver

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

May 22, 2018

FDA Warns Companies Selling "Sun Protection" Supplements

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

May 19, 2018

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

On May 18, 2018, MBI Distributing, Inc.

May 19, 2018

Sexual Enhancement Supplements Containing Undeclared Drugs Recalled

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

May 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.

July 03, 2018

FDA Warns Seller of Adulterated Chinese Herbal Supplements

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

September 01, 2018

Homeopathic Remedies Contaminated With Bacteria

On August 29, 2018, Hellolife, Inc.

September 22, 2018

MyoWhey Protein Powder Recalled

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

September 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.

December 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.

December 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.

November 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.

April 06, 2018

Workout Supplements Recalled Due To Allergen Risk

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

March 16, 2018

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

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

January 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.

January 29, 2018

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

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

January 26, 2018

Seller of Coenzyme-A Warned For Making Drug Claims

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

January 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.

December 26, 2017

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

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

December 23, 2017

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

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

February 17, 2018

FDA Warns Seller Reishi Mushroom Supplements

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

July 21, 2003

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

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

August 31, 2004

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

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

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 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. 

November 12, 2017

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

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

October 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.

October 17, 2017

Organic Tarragon Spice Recalled Due to Salmonella Risk

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

October 13, 2017

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

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

September 28, 2017

Seller of Prostate, Reishi Supplements Warned for Manufacturing Violations

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

September 26, 2017

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

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

July 18, 2017

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

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

July 11, 2017

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

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

August 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.

July 24, 2017

Protein Bars Recalled Due to Listeria Risk

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

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 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.

March 21, 2017

Twenty-one Sexual Enhancement Products Recalled

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

February 21, 2017

Sexual Enhancement Supplement Recalled

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

February 16, 2017

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

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

February 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.

February 09, 2017

Herbal Supplement Found to Contain Ephedra Alkaloids Recalled

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

February 09, 2017

Federal Court Orders Dietary Supplement Distributor to Stop Selling Its Products

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

February 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.

October 18, 2016

Seller of Sublingual Vitamins Warned for Drug Claims

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

October 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.

October 04, 2016

Turmeric Spice Recalled Due to Elevated Lead Levels

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

September 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.

September 02, 2016

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

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

August 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.

August 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.

August 08, 2016

Turmeric Spice Recall Expanded to Include More Brands

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

August 05, 2016

More Turmeric Spice Recalled

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

July 29, 2016

Ground Turmeric Spice Recalled Due to Lead Contamination

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

July 23, 2016

Maker of "Super Food" Warned for Manufacturing Violations

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

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.

June 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.

June 17, 2017

Protein Bars and Bites Recalled Due to Listeria Risk

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

June 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.

May 30, 2017

Maker of Collagen Supplement Warned for Manufacturing Violations

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

May 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.

January 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.

December 03, 2016

Male Enhancement Supplement Recalled

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

November 25, 2016

DMAA Product Recalled

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

November 19, 2016

GNC Women's Multi Recalled Due to Undeclared Allergen

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

February 23, 2016

Flax Seed and Chia Powders Recalled

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

February 06, 2016

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

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

February 03, 2016

Seller of Weight and Enhancement Supplements Warned For Drug Claims

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

January 26, 2016

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

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

January 21, 2016

Morphine Found in Licorice Product

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

January 20, 2016

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

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

January 16, 2016

Seller of Liver, Lung Support Supplements Warned for Drug Claims

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

December 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.

December 12, 2015

Sexual Enhancement Supplement Recalled

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

May 15, 2016

Sexual Enhancement Supplements Recalled

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

May 10, 2016

Multis and Energy Mixes Recalled

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

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. 

April 06, 2016

FDA Warns of Stimulant Methylsynephrine In Supplements

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

March 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.

March 15, 2016

FDA Warns Sellers of Weight and Workout Supplements Containing Acacia Rigidula

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

November 11, 2015

Consuming a Single Energy Drink May Increase Cardiovascular Risk

A recently published study found that consumption of a single caffeinated energy drink significantly increased blood pressure and noradrenaline levels in healthy young adults. The researchers noted these changes could potentially increase the risk of cardiovascular events.

September 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.

September 18, 2015

High Levels of Mercury and Lead Found in Ayurvedic Herbal Supplements

On September 17, 2015, the FDA announced that Shree Baidyanath Ayurved Bhawan Ayurvedic dietary supplements were found to contain high levels of lead and/or mercury, which can cause serious health problems.

May 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.

September 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.

August 22, 2015

Synthetic Amphetamine, Less Protein and More Sugar Than Claimed Found in Workout Supplements

On August 7, 2015, the FDA issued a warning letter to New Dawn Nutrition, Inc.

August 04, 2015

Whey, Casein and Colostrum Products Recalled

On August 3, 2015, Nutrition Resource Services, Inc. issued a voluntary recall of certain Just Be Natural (JBN) and Gifted Nutrition powders containing whey concentrate, whey isolate, casein, and colostrum because they contain undeclared milk.

July 28, 2015

Abnormal Heart Rhythms Linked with Unauthorized Natural Product, Health Canada Warns

On July 27, 2015, Health Canada (the Canadian equivalent of the U.S. FDA) announced that it has received a serious adverse reaction report of abnormal heart rhythms associated with the use of an unauthorized natural product in Canada called Remogen, which contains the drug ibogaine.

July 12, 2015

Marketers of Memory Supplement to Pay $1.4 Million to Settle FTC Charges

On July 8, 2015, the FTC announced the marketers of Procera AVH (Brain Research Labs Inc.) have agreed to pay $1.4 million to settle charges they made deceptive claims that the supplement could significantly improve memory, mood and cognitive function.

July 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.

June 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.

May 26, 2015

Skin Measurement Device Used to Select Nutritional Supplements Not Approved for This Use, FDA Warns

On May 8, 2015, the FDA issued a warning letter to ZYTO Technologies, Inc.

May 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.

May 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).

May 13, 2015

Amberen Weight Loss Claims Not Supported by Evidence, Says FTC

On May 12, 2015, the FTC announced it filed a complaint to stop Lunada Biomedical Inc. from advertising that its product Amberen is clinically proven to cause substantial weight loss in women over 40.

April 29, 2015

FDA Targets Weight Loss and Workout Supplements Listing Synthetic Stimulant DMBA

On April 24, 2015, the FDA issued warning letters to sellers of weight loss and workout supplements that list a synthetic, amphetamine-like compound called 1,3-dimethylbutylamine (DMBA) on product labels. 

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.

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 28, 2006

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

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

October 15, 2007

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

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

June 21, 2005

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

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

September 16, 2005

FTC Stops Weight-loss Claims about Seaweed-based Patches

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

September 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 ...

June 23, 2003

FDA Warns Consumers Against Taking 6 Sexual Enhancement Supplements

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

May 17, 2002

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

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

May 03, 2002

More Information on Recall of PC-SPES - Prostate Supplement

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

March 28, 2011

FDA Cracks Down on Violators of Supplement Manufacturing Rules

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

July 19, 2011

FDA Warns of Unsafe Drug in Slimming Supplements

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

October 08, 2010

FDA Warns of Stimulant in Slimming Capsules

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

February 24, 2011

Recall of Counterfeit Extenze Tablets Containing Drugs

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

January 17, 2012

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

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

October 05, 2011

FDA Warns Herbal Nitro of Manufacturing Violations

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

June 21, 2011

FDA Warns Laboratory of Manufacturing Violations

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

June 07, 2011

FDA Seizes Elderberry Juice Concentrate Due to Unproven Claims

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

June 01, 2011

FDA Finds Pesticides in Ginseng Supplement

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

March 03, 2012

Seller of Cancer Cures Warned by FDA

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

March 09, 2012

Maker of Inhaled Caffeine Product Gets Warning

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

April 16, 2012

Protein Supplement Maker Fails FDA Audit -- Many Products Affected

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

March 02, 2012

Recall of Enhancement Supplement for Men -- Contains Drug

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

February 17, 2012

FDA Warns Supplement Company of Manufacturing Violations

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

February 16, 2012

Recall of Enhancement Supplement for Women -- Contains Drug

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

February 11, 2012

Herbal Sprays for Colds and Cold Sores Recalled

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

December 14, 2009

Nationwide Recall of Sexual Enhancement Supplements Containing Drug-like Compound

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

September 13, 2010

ExtenZe Enhancement Supplements Seized in Canada

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

June 24, 2010

FDA Warns Seller of Pills Used to Treat Autism

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

May 03, 2010

FDA Warns Consumers to Avoid Breath Supplement Contaminated with Lead

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

April 07, 2010

Nationwide Recall of Masxtreme Capsules Containing Drugs with Cardiovascular Side Effects

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

February 17, 2010

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

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

August 28, 2008

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

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

March 19, 2009

QVC Settles Charges of False Claims for Supplements

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

May 17, 2007

Recall of Shark Cartilage Due to Potential Contamination

On May 16, 2007, NBTY, Inc.

June 28, 2014

Chia Seed Recall Expanded

On June 26, 2014, HEALTH MATTERS AMERICA INC.

June 12, 2014

Marketers of Memory Supplement Settle FTC Charges of Deceptive Claims

Martek Biosciences Corporation and i-Health Inc., marketers of BrainStrong Adult, have agreed to settle Federal Trade Commission (FTC) charges that claims the supplement could improve adult memory and prevent cognitive decline were deceptive, and not supported by sufficient clinical evidence.

June 05, 2014

More Chia Powders Recalled Due to Salmonella Risk

On June 4, 2014, Health Matters America Inc. issued a voluntary recall its Organic Traditions Sprouted Chia Seed Powder and Organic Traditions Sprouted Chia & Flax Seed Powder because they have the potential to be contaminated with Salmonella.

May 31, 2014

Sellers of "Cancer" Supplements Warned for Drug Claims

Two sellers of graviola supplements promoted to treat cancer have been issued warning letters by the FDA. Graviola (Annona muricata), also known as soursop, is the fruit of a tree native to South America and Puerto Rico.

May 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.

May 29, 2014

Recall of Sexual Enhancement Supplements Expanded

On May 28, 2014, Eugene Oregon, Inc. expanded its previous recall of certain lots of sexual enhancement supplements African Black Ant, Black Ant, and Mojo Risen. All lots of these supplements are now recalled.

May 21, 2014

Seller of Gingko and Milk Thistle Warned for Manufacturing Violations and Drug Claims

On April 4, 2014, the FDA issued a warning letter to Xtra Life Natural Systems, Inc.

October 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.

October 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.

September 30, 2014

U.S. Marshals Seize $5 Million Worth of Kratom

On September 25, 2014, U.S. Marshals seized more than 25,000 pounds of raw kratom valued at over $5 million from Rosefield Management, Inc. in Van Nuys, California. The action was taken at the request of the FDA.

September 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.

September 09, 2014

Maker of Popular Green Coffee Bean Extract Settles FTC Charges of Unsupported Weight Loss Claims

Applied Food Sciences, Inc., maker of green coffee bean extract GCA, has agreed to pay $3.5 million to settle FTC charges that weight loss claims made about the extract were not supported by scientific evidence.

August 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.

July 30, 2014

Chocolate and Carob Drink Mix Recalled Due To Salmonella Risk

On July 25, 2014, CaCoCo, Inc. issued a recall of CaCoCo Original and Global Warrior chocolate drink mixes because they contain organic carob powder which has the potential to be contaminated with Salmonella.

July 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.

July 26, 2014

FTC Says Company Made "Outrageous" Weight Loss Claims

Marketers for the Canadian-based Freedom Center Against Obesity have agreed to pay $500,000 to settle FTC charges the company made deceptive claims about its Double Shot diet pills.

December 07, 2014

FDA Raises Concerns Over Generic ADHD Drugs

On November 13, 2014, the U.S.

February 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.

January 31, 2015

Protein Powder Recalled Due to Food Poisoning Risk

On January 30, 2015, Aloha, Inc. issued a voluntary recall of all packages of Premium Protein powder blends in chocolate and vanilla because they have the potential to be contaminated with Staphylococcus enterotoxin .

January 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.

January 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.

January 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.

January 21, 2015

Smoothie Blends Recalled Due to Potential Listeria Contamination

On January 18, 2015, Inventure Foods, Inc. issued a recall of RADER FARMS Fresh Start Smoothie Blend, Fresh Start Sunrise Refresh Fusion, and Fresh Start Daily Power Fusion, because they have the potential to be contaminated with Listeria monocytogenes.

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.

January 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.

December 20, 2014

Weight Loss Supplement Recalled

On December 19, 2014, Bethel Nutritional Consulting, Inc. issued a recall of one lot of weight loss supplement SLIM-K Capsules because they were found to contain sibutramine.

December 20, 2014

Company Recalls Second Weight Loss Supplement

On December 19, 2014, Bethel Nutritional Consulting, Inc. issued a recall of one lot of weight loss supplement B-Lipo Capsules because they were found to contain Lorcaserin.

April 09, 2014

Maker of Relaxation Drink Warned For Melatonin Ingredient

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

August 06, 2013

Weight Loss Supplement Recall Expanded

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

August 27, 2013

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

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

August 23, 2013

Sexual Enhancement Supplement Containing Undeclared Drugs Recalled

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

August 16, 2013

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

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

December 26, 2013

Weight Loss Supplement Recalled

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

December 19, 2013

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

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

December 16, 2013

Weight Loss Capsules Recalled Due Allergen Risk

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

December 13, 2013

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

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

November 21, 2013

Weight Loss Supplement Recalled

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

November 20, 2013

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

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

October 12, 2013

Metagenics Enzyme Supplement Recalled Due To Drug Risk

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

October 11, 2013

Prebiotic and Digestive Enzyme Supplement Recalled Due To Drug Risk

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

September 27, 2013

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

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

February 19, 2014

Seller of Sexual Enhancement Supplements Warned For Manufacturing Violations

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

February 13, 2014

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

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

January 16, 2014

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

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

March 31, 2014

Seven Sexual Enhancement Supplements Recalled Due to Undeclared Drugs

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

January 04, 2014

Smoking Cessation and Anti-Inflammatory Supplements Contain Unapproved Ingredient

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

July 11, 2014

Maker of Cough and Sleep "Remedies" Warned for Drug Claims

On June 27, 2014, the FDA issued a warning letter to Zarbee's, Inc.

November 17, 2014

Probiotic Powder Recalled

On November 14, 2014, Solgar, Inc. issued a voluntary recall of Solgar ABC Dophilus Powder (NET Wt. 1.75 oz (50 g)) because it was found to contain Rhizopus oryzae, a fungus which may cause Mucormycosis infection.

November 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.

May 07, 2014

Three Sexual Enhancement Supplements Recalled

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

May 01, 2014

Weight Loss Supplement Recalled

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

April 29, 2014

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

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

April 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.

April 18, 2014

FDA Questions Ingredient in Workout Supplement

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

February 14, 2013

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

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

February 12, 2013

Judge Orders Drug and Supplement Company to Cease Manufacturing and Distribution

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

January 30, 2013

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

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

January 18, 2013

Recall: Iron Supplement Containing Motion Sickness Drug

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

March 22, 2013

Maker of Nutrition Shakes Warned For Manufacturing Violations

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

March 21, 2013

Probiotic Recalled Due To Undeclared Soy

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

March 13, 2013

Recall: Male Sexual Enhancement Supplement Containing Drugs

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

March 11, 2013

Nutrition Bar Recalled Due To Undeclared Allergen

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

March 06, 2013

Protein Bar Recalled Due To Salmonella Risk

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

August 29, 2013

Seller of CELLFOOD Supplements Warned For Manufacturing Violations and Drug Claims

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

May 03, 2013

Homeopathic Company Warned For Drug Claims and Improper Labeling

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

June 12, 2013

Weight Loss Supplement Recalled Due To Undeclared Drugs

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

June 07, 2013

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

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

May 29, 2013

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

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

May 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.

May 23, 2013

Maker of Liver Detox and Insulin Supplements Warned For Drug Claims

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

May 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.

May 17, 2013

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

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

April 18, 2013

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

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

April 11, 2013

Maker of Workout Booster Warned For Manufacturing Violations

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

April 10, 2013

Recall: Sexual Enhancement Supplement Containing Undeclared Drug

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

July 12, 2013

Herbal Supplement Company Warned For Drug Claims, Manufacturing Violations

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

July 05, 2013

Seller of Vision Supplement Warned For Drug Claims

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

September 07, 2012

Prebiotics Recalled For Salmonella Risk

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

September 21, 2012

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

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

September 18, 2012

Men’s Sexual Enhancement Supplement Containing Prescription Drug Recalled

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

September 18, 2012

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

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

October 18, 2012

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

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

August 09, 2012

Makers of Mineral Water Containing Lithium Warned

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

August 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.

November 21, 2012

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

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

October 24, 2012

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

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

February 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.

December 19, 2012

Sexual Enhancement Supplements Recalled Due To Undeclared Drugs

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

February 20, 2013

Cold, Flu and Stress Supplement Company Warned For Adulteration, Drug Claims And More

On October 5, 2012, the FDA issued a warning letter to dietary supplement manufacturer Wholistic Herbs, Inc. following a facility inspection which found the company's products, including At-Ease, Morning Calm, Aller-Ban, Stomach Flu, Kold & Koff, Kold Sore, and L.

October 24, 2012

Manufacturer of Green Tea, Vitamin E, Omega-3 and Cranberry Supplements Warned For Manufacturing Violations, Misbranding and Drug Claims

On October 16, 2012, the FDA issued a warning letter to dietary supplement manufacturer Advanced Nutritional Technology Inc.

November 02, 2012

Manufacturer of Prostate, Inflammation and Cholesterol Supplements Warned For Drug Claims

On October 15, 2012, the FDA issued a warning letter to Ortho Molecular Products, Inc. for making drug claims about the following dietary supplements: Candicid Forte, Inflamma-bLOX, Lipitrol, Mucosagen, Prostatrol Forte, Resvoxitrol, Paracid Forte, VascuPak HTN and Lithium Orotate.

July 27, 2012

Prescription and Street Drug Alternatives Found in Male Enhancement, Mood, and Sleep Supplements

On July 10, 2012, the FDA issued a warning letter to Evol Nutrition Associates, Inc. subsequent to a 2011 inspection which found a number of the company's products contained prescription and investigational drugs and were misbranded.

August 30, 2012

Supplement Company Warned For Medical Claims and Misbranding Of Omega-3, CoQ10, Noni Juice And More

On July 12, 2012, the FDA issued a warning letter to Alfa Vitamins Laboratories, Inc.

May 03, 2013

Maker of Omega-3, Saw Palmetto, St. John’s Wort Supplements And More Warned For Manufacturing Violations and Drug Claims

On March 19, 2013, the FDA issued a warning letter to Sunset Natural Products Inc.

May 10, 2013

Maker of Concentration, Pain, Immune, Cholesterol Supplements Warned For Drug Claims

On April 24, 2013, the FDA issued a warning letter to EuroPharma Co., Inc., following a review of the company's website which found statements made about Calm Kids, CholestCaps, CuraMed 375 mg, CuraMed 750 mg, Curamin, Mental Advantage, Tri-Iodine, and Viragen to be drug claims.

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.

April 16, 2014

Weight Loss Supplements Found To Contain Prescription Antidepressant and Other Drugs

On March 7, 2014, the FDA issued a warning letter to Deseo Rebajar Inc. because the company's following weight loss products were found to contain drugs:

January 09, 2014

Four Companies Settle FTC Charges of Deceptive Weight Loss Claims

On January 7, 2014, the Federal Trade Commission (FTC) announced that marketers for four weight loss products have agreed to settlements over charges of deceptive weight loss claims.

September 13, 2013

Metagenics Warned For Misbranding of Medical Foods and Drug Claims

On August 13, 2013, the FDA issued a warning letter to Metagenics, Inc.

August 16, 2013

Ginkgo, Milk Thistle, Cleanse and Nopal Supplement Maker Warned For Manufacturing Violations, Drug Claims

On July 23, 2013, the FDA issued a warning letter to Natural Products Services, Inc.

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.

December 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.

February 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.

September 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.

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.

December 30, 2007

FDA Warns Consumers Not to Use Several "Shangai" Sexual Enhancement Supplements

On December 28, 2007, the U.S. Food and Drug Administration (FDA) advised consumers not to buy or use Super Shangai, Strong Testis, Shangai Ultra, Shangai Ultra X, Lady Shangai, and Shangai Regular, also marketed as Shangai Chaojimengnan, products.

February 27, 2009

$4 Million Settlement by Supplement Maker for False Claims

On February 26, 2009, the Texas Attorney General announced that an agreement was reached with Mannatech Inc. and its former CEO, Samuel L. Caster, both of which had been charged with orchestrating an unlawful marketing scheme that exaggerated their products’ health benefits.

July 29, 2008

Recall of Sexual Enhancement Supplements Containing Drug

On July 28, 2008 the U.S. FDA announced that Jack Distribution, LLC and G & N works, Inc. are conducting a voluntary nationwide recall of all lot numbers of the company's supplement products sold under the brand names Rize 2 The Occasion and Rose 4 Her.

July 28, 2008

Seizure of Xiadafil VIP Tablets After Company Refuses Recall

On July 24, 2008, the FDA announced that U.S. Marshals seized nearly $74,000 worth of Xiadafil VIP tablets, Lots 6K029 and 6K209-SEI, distributed by SEI Pharmaceuticals, Inc. of Miami, Fla.

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.

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.

July 29, 2009

FDA Warns Against Body Building Supplements with Steroid-like Compounds

On July 28, 2009, the U.S. FDA notified the public about new safety information concerning products marketed for body building and increasing muscle mass.

May 28, 2003

Warning and Recall for "Herbal" Sexual Enhancement Supplement in Canada Illegally Containing Pharmaceutical Compound

On May 27, 2003 - Health Canada warned consumers not to use Hua Fo VIGOR-MAX tablets, a Chinese herbal product that contains tadalafil.

March 11, 2003

Rexall Agrees to Pay up to $12 million to Users of Misleading Cellulite Supplement

On March 11, 2003, the Federal Trade Commission (FTC) reported that Rexall Sundown, Inc. (Rexall) will pay up to $12 million to resolve FTC charges regarding its marketing of the dietary supplement, "Cellasene," a purported cellulite treatment product.

December 22, 2005

Health Canada Warns Consumers Not to Take Chaparral

On December 21, 2005, Health Canada (Canada's health ministry) warned consumers not to ingest the herb chaparral in the form of loose leaves, teas, capsules or bulk herbal products because of the risk of liver and kidney problems.

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.

March 16, 2006

Garden of Life, Maker of Primal Defense, Settles FTC Charges

On March 9, 2006, The Federal Trade Commission (FTC) announced that an operation that marketed dietary supplements sold at Whole Foods Market, GNC, the Vitamin Shoppe, and on the Internet settled FTC charges that they made deceptive advertising claims about their supplements.

June 17, 2004

FTC Challenges Deceptive Weight Loss Claims for Supplement Targeted at Hispanics

On June 17, 2004, the Federal Trade Commission (FTC) announced a new law enforcement action challenging false advertising for the 1-2-3 Diet Kit, a purported weight loss product.

January 18, 2005

Sellers of “Fat Trapper Plus” and “Exercise in a Bottle” Banned from Advertising Weight-Loss Products

On January 18, 2005, the Federal Trade Commission (FTC)announced that Enforma Natural Products, Inc.

January 05, 2005

Marketers of Brain-Rejuvinating Supplement Settle FTC Charges of False Claims

On January 5, 2005, the U.S. Federal Trade Commission (FTC) announced that a company that heavily advertised an herbal dietary supplement called "Sagee" to the Chinese-language and Vietnamese-language communities had settled FTC charges of making false and unsubstantiated claims for the product.

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.

July 30, 2003

Maker of Weight-Loss and Cellulite Treatment Ordered to Stop False Claims and Pay Consumer Redress

On July 30, 2003 the Federal Trade Commission (FTC) reported that a Canadian-based company operating in the United States under the name “Bio Lab,” and its president, Jean-Francois Brochu, have agreed to settle FTC charges that they deceived consumers through false and unsubstantiated advertising ...

June 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.

August 07, 2015

Male Enhancement and Weight Loss Supplement Containing Drugs Recalled

On August 6, 2015 Blue Square Market Inc. issued a recall of the following supplements which were found to contain undeclared drugs: