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News Release
August 05, 2008
ConsumerLab.com Find Fifty Fish Oil Supplements Pass Quality Testing -- New Report Helps Consumers Choose Among Pills, Liquids, Foods and Beverages with Omega-3 Fatty Acids (EPA and DHA)
WHITE PLAINS, NEW YORK — AUGUST 5, 2008 — ConsumerLab.com announced today that testing of fifty omega-3 fish oil supplements, foods or beverages (including two marketed for pets) found all to have safe levels of mercury, lead and PCBs.
Recalls & Warnings
July 23, 2025
FDA Warns Seller of Allegro Eye Drops, Tea Tree Oil Eyelid Wipes, and More
On July 9, 2025, the FDA issued a Warning Letter to Scope Health Inc.
Recalls & Warnings
October 16, 2025
More Ground Cinnamon Found to Contain Lead
On October 10, 2025, the FDA warned consumers not to consume three brands of ground cinnamon, which were found to contain elevated levels of lead. This brings the total to 16 brands that the agency has included in its public health alert about lead in cinnamon.
Recalls & Warnings
January 13, 2026
Sea Moss Gel Superfood Recalled Due to Possible Health Risk
On January 9, 2026, Diva Fam Inc.
Recalls & Warnings
November 03, 2025
More Ground Cinnamon Recalled Due to Lead
On October 30, 2025, the FDA updated its public health alert on ground cinnamon to include two additional products found to contain elevated levels of lead: DEVI Cinnamon Powder and BaiLiFeng Dried Cinnamon Powder.
Recalls & Warnings
September 25, 2025
StellaLife Warned by FDA for “Homeopathic” Rinses and Oral Care Products
On September 5, 2025, the FDA issued a Warning Letter to Stellalife, Inc.
Recalls & Warnings
June 04, 2026
Amare Global Sued for Supplement Claims for Depression, Anxiety, and ADHD
On June 2, 2026, the Federal Trade Commission (FTC) sued Amare Global Holdings Inc. and three of its principals for allegedly misrepresenting that its dietary supplements marketed for children and adults could treat or cure health conditions such as depression, anxiety, and ADHD.
News Release
March 13, 2006
ConsumerLab.com reports on supplements for bone health containing calcium and vitamin D— Results posted for 32 supplements for adults and children; One found contaminated with lead
WESTCHESTER COUNTY, NEW YORK — MARCH 13, 2006 — ConsumerLab.com announced test results today from its new Product Review of Supplements for Bone Health covering 32 adult and children's products containing calcium and vitamin D. Sales of calcium supplements in the U.S.
Recalls & Warnings
May 09, 2025
Organic Traditions Pumpkin Seeds Recalled in U.S. and Canada
On May 8, 2025, Advantage Health Matters Inc. recalled packages of Organic Traditions Organic Jumbo Pumpkin Seeds in the U.S. and Canada because they have the potential to be contaminated with Salmonella.
Recalls & Warnings
May 28, 2026
More Moringa Recalled Due to Salmonella Risk
On May 26, 2026, Total Nutrition Inc. recalled certain lots of TNVitamins Ultra Potent Complete Green Superfood Moringa and Doctor’s Pride Complete Green Superfood Ultra Potent Moringa capsules because they may be contaminated with Salmonella.
Recalls & Warnings
June 10, 2025
Zicam and Orajel Swabs Recalled
On June 6, 2025, Church & Dwight Co., Inc. recalled all lots within expiry of Zicam Cold Remedy Nasal Swabs, Zicam Nasal AllClear Swabs, and Orajel Baby Teething Swabs due to potential microbial contamination identified as fungi in the cotton swab components.
Recalls & Warnings
May 04, 2026
Nupack Nutrition Warned for Manufacturing Violations, Claims about Psyllium and Maca
On March 20, 2026, the Food and Drug Administration issued a Warning Letter to Nupack Inc.
Recalls & Warnings
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.
Recalls & Warnings
March 13, 2025
FTC Sends Refund Checks to Consumers of Pure Green Coffee Supplement
On March 6, 2025, the Federal Trade Commission (FTC) announced it is mailing 39,977 checks totaling more than $905,000 to consumers who purchased Pure Green Coffee, to settle charges the product was promoted with deceptive health claims and marketing practices.
Recalls & Warnings
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.
Recalls & Warnings
June 10, 2024
StellaLife Homeopathic Oral Rinse & Spray Recalled Due to Yeast, Mold, and Bacteria
On June 5, 2024, HomeoCare Laboratories, Inc.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
September 14, 2023
FDA Warns CVS, Walgreens, Similasan & Others for Eye Drop Violations
On September 11, 2023, the FDA issued Warning Letters to the following eight sellers of homeopathic and other types of eye drops regarding the products noted in italics due to a variety of violations of FDA regulations, most notably that they were marked with claims suggesting that they could cure, ...
Recalls & Warnings
January 04, 2024
Toxic Herb Found in More Tejocote Root Supplements
On January 3, 2024, the FDA warned consumers not to purchase or use certain tejocote root supplements after FDA laboratory analysis confirmed the products contain yellow oleander (Thevetia peruviana), a toxic herb.
Recalls & Warnings
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).
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
April 25, 2022
Some OTC Skin Lighteners Contain Potentially Harmful Ingredient, Warns FDA
On April 19th, 2022, the FDA issued warnings to 12 companies for selling over-the-counter (OTC) skin-lightening products containing hydroquinone.
Recalls & Warnings
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.
Recalls & Warnings
November 21, 2022
Healthy Sense and People’s Choice Multis Recalled
On November 17, 2022, Mason Vitamins Inc.
Recalls & Warnings
June 02, 2022
Walmart Inc. Recalls Joint Supplements With Omega-3, Glucosamine & Curcumin
On May 28, 2022, Walmart Inc. issued a voluntary recall of all lots of Artri Ajo King Joint Supplements after FDA laboratory analysis found the presence of undeclared diclofenac.
Recalls & Warnings
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.
Recalls & Warnings
March 13, 2020
FDA Finds Problems at 52% of Supplement Manufacturing Sites in U.S. and 42% Abroad
ConsumerLab.com has obtained results of the FDA's inspections in Fiscal Year 2019 (October 1, 2018 - September 30, 2019) of 598 dietary supplement manufacturing facilities in the U.S.
Recalls & Warnings
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).
Recalls & Warnings
May 29, 2021
FDA, FTC Warns Five Sellers of "Infertility" Supplements
The FDA and FTC (Federal Trade Commission) sent warning letters to the following five companies in May for illegally selling dietary supplements promoted with claims to treat infertility and other reproductive health issues:
Recalls & Warnings
March 05, 2021
FTC Takes Further Action Against Deceptive CBD Claims
On March 5, 2021, the Federal Trade Commission (FTC) announced that it has approved final administrative consent orders against six companies for selling CBD products with unsupported and deceptive health claims that they can treat a variety of conditions, including cancer, heart disease, ...
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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).
Recalls & Warnings
August 13, 2020
FDA Warns Three More Companies Selling Unapproved COVID-19 Tests
Between July 23 and 24, the FDA issued warning letters to three companies for marketing unapproved, adulterated or misbranded antibody tests for coronavirus (COVID-19).
Recalls & Warnings
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.
Recalls & Warnings
May 09, 2020
FTC Warns 45 More Companies for Coronavirus Claims
On May 7, 2020, the FTC announced that it sent warning letters to 45 companies for selling products such as herbal products, immune system boosters, and vitamin C with unsupported claims that they can treat coronavirus (COVID-19).
Recalls & Warnings
April 28, 2020
Ten Multi-Level Marketing Companies Warned for Coronavirus and Deceptive Earnings Claims
On April 24, 2020, the FTC announced that it sent warning letters to ten multi-level marketing companies for selling products such as essential oils and immune system boosters with unsupported claims that they can treat coronavirus (COVID-19) and/or for misrespresenting potential earnings people ...
Recalls & Warnings
August 14, 2020
The Green Herb and New Genesis Health Warned for Manufacturing Violations
On July 31, 2019, the FDA issued a warning letter to Davis Ventures, Inc.
Recalls & Warnings
December 17, 2020
FTC Crackdown on Six Deceptive CBD Products
On December 17, 2020, the FTC announced that it is taking action against six companies for selling CBD products with unsupported and deceptive health claims that they can treat a variety of conditions, including cancer, heart disease, hypertension, Alzheimer's disease, and others.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
June 16, 2020
FDA Warns Four Companies for Unsafe "Homeopathic" Injectables
On June 16, 2020, the FDA issued warning letters to four manufacturers of unapproved injectable drugs labeled as homeopathic.
Recalls & Warnings
June 09, 2020
Six More Multi-Level Marketing Companies Warned for Coronavirus and Deceptive Earnings Claims
On June 5, 2020, the FTC announced that it sent warning letters to six multi-level marketing companies for selling products such as immune system boosters and probiotics with unsupported claims that they can treat coronavirus (COVID-19) and/or for misrepresenting potential earnings people who have ...
Recalls & Warnings
May 23, 2020
FTC Warns 50 More Companies for Coronavirus Claims
On May 21, 2020, the FTC announced that it sent warning letters to 50 companies for selling products such as herbal products, immune system boosters, and vitamin C, with unsupported claims that they can treat coronavirus (COVID-19).
Recalls & Warnings
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).
Recalls & Warnings
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.
Recalls & Warnings
October 06, 2005
Deceptive Marketing of “Supreme Greens" -- Settlement with FTC
On October 6, 2005, the Federal Trade Commission (FTC) announced that three individuals and two companies have settled FTC charges over their roles in the deceptive marketing of Supreme Greens, an herbal supplement.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
February 01, 2018
Seller of Supplements for Opiate Withdrawal Warned for Drug Claims
On January 11, 2018, the FDA sent warning letters to ten sellers of supplements promoted to treat opiate withdrawal following reviews of the companies' websites and social media which found statements and testimonials made about the products to be drug claims.
Recalls & Warnings
April 25, 2017
Beware of Products Which Promise to Treat or Cure Cancer, FDA Warns
On April 25, 2017, the FDA warned consumers to be aware of supplements and other products claiming to cure cancer.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.).
Recalls & Warnings
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:
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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 ...
Recalls & Warnings
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.
Recalls & Warnings
April 21, 2011
FTC Targets Fake News Sites Making Deceptive Acai Claims
On April 19, 2011, the Federal Trade Commission (FTC) requested federal courts to temporarily halt the allegedly deceptive tactics of 10 operations using fake news websites to market acai berry weight-loss products.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
June 04, 2004
FTC Charges Marketers of Two Supplements with False Claims to Cure Range of Diseases
On June 3, 2004 the Federal Trade Commission (FTC) charged marketers of two dietary supplements with falsely claiming that their products can prevent and cure cancer and other diseases. According to the FTC’s complaint, Boston-area marketers Direct Marketing Concepts, Inc. (DMC), ITV Direct, Inc.
Recalls & Warnings
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.
Recalls & Warnings
October 05, 2007
FTC Charges Progesterone Cream Sellers with Making Unsubstantiated Claims
On October 5, 2007 the Federal Trade Commission (FTC) announced complaints against seven online sellers of alternative hormone replacement therapy (HRT) products, alleging that they made health claims for their natural progesterone creams without supporting scientific evidence.
Recalls & Warnings
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 ...
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
April 23, 2019
"Brain Boosting" Supplements Were Promoted With Non-Existent Clinical Studies
On April 10th, 2019, the FTC (Federal Trade Commission) announced the marketers of cognitive enhancement supplements Geniux, Xcel, EVO, and Ion-Z have agreed to settle charges that they made false claims about the product, including fake research references and celebrity ...
Recalls & Warnings
July 15, 2010
Supplement Company Pays $5.5 Million to Settle False Advertising Claims
On July 14, 2010, the Federal Trade Commission (FTC), as part of its ongoing efforts to stop bogus health claims, announced that it is requiring a major marketer of dietary supplements to pay $5.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
May 20, 2014
FTC Charges Seller of Green Coffee Bean with False Weight Loss Claims, Fake Websites
On May 15, 2014, the Federal Trade Commission (FTC) filed a lawsuit against the sellers of Pure Green Coffee for making unsubstantiated weight loss claims and deceiving consumers with fake "news" websites.
Recalls & Warnings
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:
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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 ...
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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 ...
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
January 10, 2012
Acai Berry Pill Marketers to Pay $1.5 Million to Settle FTC Charges
On January 9, 2012, the U.S. Federal Trade Commission (FTC) announced that an operation that marketed acai berry supplements, "colon cleansers," and other products using allegedly fraudulent free trial offers and phony endorsements from Oprah Winfrey and Rachael Ray will pay $1.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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.
Recalls & Warnings
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).
Recalls & Warnings
March 02, 2013
FDA Finds Manufacturing Violations At NSF-Certified Supplement Facility
The FDA recently warned dietary supplement manufacturer Beehive Botanicals, Inc.
Recalls & Warnings
April 11, 2015
Acai Berry Marketers Who Tricked Consumers with Fake News Sites Ordered to Pay $16 Million
On April 6, 2015, the Federal Trade Commission (FTC) announced that a recent U.S. district court ruling will require marketing affiliates for LeanSpa's acai berry and "colon cleanse" weight loss products to pay $16 million in consumer redress.
Recalls & Warnings
September 05, 2015
Powdered Caffeine Risky, FDA Warns
On August 27, 2015, the FDA issued a warning letter to five companies selling caffeine powder, warning that the powder "presents a significant or unreasonable risk of illness or injury under the conditions of use recommended or suggested in the labeling."
Recalls & Warnings
March 31, 2018
Supplement Manufacturer Shut Down for Manufacturing Violations
On March 29, 2018, the FDA announced that U.S. District Court for the Eastern District of New York has entered a consent decree of permanent injunction with Riddhi USA, Inc. and Mohd M. Alam, president and owner of Riddhi USA, Inc., for selling adulterated and misbranded dietary supplements.
Recalls & Warnings
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.
Recalls & Warnings
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.
