Notices from government agencies, such as the Food and Drug Administration (FDA) and the Federal Trade Commission (FTC), to let consumers know about recalls, tainted products, and other alerts/advisories.
2020
- Public Health Alert Concerning Nopalina Flax Seed Powder and Nopalina Flax Seed Capsules and Salmonella Contamination (FDA 01/23/20)
- ABH NATURE’S PRODUCTS, INC, ABH PHARMA, INC., and STOCKNUTRA.COM, INC. Issues Nationwide Recall of All Lots of Dietary Supplement Products (FDA 01/23/20)
2019
- Motto International Corp. Issues Voluntary Recall of Bull Platinum 30000, Stallion Platinum 30000, Rhino 7 Platinum 30000, and Panther Platinum 30000, Due to Presence of Undeclared Tadalafil (FDA 12/19/19)
- FTC, State of Maine File Contempt Action against Dietary Supplement Marketers (FTC 12/19/19)
- FTC Sending Additional Refund Checks to Consumers Who Bought LeanSpa Products (FDA 12/16/19)
- FDA underscores that consumers should not use drugs, dietary supplements and devices recalled from Basic Reset and Biogenyx following consent decree for federal violations (FDA 12/11/19)
- FDA warns 15 companies for illegally selling various products containing cannabidiol as agency details safety concerns (FDA 11/25/19)
- Med Man Issues Voluntary Nationwide Recall of Up2 Due to Presence of Undeclared Sildenafil (FDA 11/08/19)
- FDA, FTC warn company marketing unapproved cannabidiol products with unsubstantiated claims to treat teething and ear pain in infants, autism, ADHD, Parkinson’s and Alzheimer’s disease (FDA 10/22/19)
- JaDera PLUS contains hidden drug ingredients (FDA 10/06/19)
- Green Lumber contains hidden drug ingredient (FDA 09/19/19)
- Fitoterapia USA Inc. Issues Voluntary Nationwide Recall of MERO MACHO ARTIFICIAL PASSION FRUIT FLAVORED VITAMIN C LIQUID SUPPLEMENT Due to Presence of Active Ingredient Tadalafil (FDA 09/16/19)
- FTC Sends Warning Letters to Companies Advertising Their CBD-Infused Products as Treatments for Serious Diseases, Including Cancer, Alzheimer’s, and Multiple Sclerosis (FTC 09/10/19)
- Anaconda Strong Formula contains hidden drug ingredient (FDA 09/09/19)
- Lung Leader contains hidden drug ingredient (FDA 09/09/19)
- La Pepa Negra contains hidden drug ingredient (FDA 09/09/19)
- Lanugar contains hidden drug ingredients (FDA 09/06/19)
- Love in S contains hidden drug ingredients (FDA 09/06/19)
- Mero Macho contains hidden drug ingredient (FDA 09/06/19)
- Sheaya Lender contains hidden drug ingredients (FDA 09/06/19)
- LOBO contains hidden drug ingredient (FDA 09/06/19)
- Federal judge enters consent decree against Tennessee drug, dietary supplement and device distributors, Basic Reset and Biogenyx, for drug, device and dietary supplement violations (FDA 09/03/19)
- Mountain Mel’s Essential Goods, LLC Recalls The Milk Lady’s Herbal Tea Blend, Peaceful Baby Herbal Tea Blend, and Diges-teas Herbal Tea Blend, Because of Possible Health Risk (FDA 08/29/19)
- FTC Refunds Consumers Who Bought FlexiPrin Joint Pain Supplement (FDA 08/22/19)
- FDA warns consumers about the dangerous and potentially life threating side effects of Miracle Mineral Solution (FDA 08/12/19)
- FDA warns company marketing unapproved cannabidiol products with unsubstantiated claims to treat cancer, Alzheimer’s disease, opioid withdrawal, pain and pet anxiety (FDA 07/23/19)
- FDA advises patients not to use Herbal Doctor Remedies’ medicines (FDA 07/23/19)
- Public Notification: Big Penis contains hidden drug ingredient (FDA 07/16/19)
- DaVinci Laboratories Issues Allergy Alert on Undeclared Fish Allergen in Omega-3 1000 Product Lot 35532200 (FDA 07/11/19)
- Statement on warning for women of childbearing age about possible safety risks of dietary supplements containing vinpocetine (FDA 06/03/19)
- STIFF BOY LLC. Issues Voluntary Nationwide Recall of THE BEAST Capsules Due to Presence of Undeclared Sildenafil (FDA 05/08/19)
- Geniux Dietary Supplement Sellers Barred from Unsupported Cognitive Improvement Claims (FDA 04/10/19)
- SD Import Issues Voluntary Nationwide Recall of Aphrodisiac Capsules Due to Presence of Undeclared Sildenafil (FDA 04/09/19)
- USA LESS Issues Voluntary Nationwide Recall of LEOPARD Miracle Honey Due to Presence of Undeclared Sildenafil (FDA 03/22/19)
- Kingston Pharma, LLC RECALLS " DG™/health NATURALS baby Cough Syrup + Mucus” Because of Possible Health Risk (FDA 03/20/19)
- Sunstone Organics Issues Voluntary Nationwide Recall of Select Kratom Products Due to Potential Contamination by Salmonella (FDA 03/01/19)
- Golean Detox USA Issues Voluntary Nationwide Recall of Golean DETOX Capsules Due to Presence of Undeclared Sibutramine and Phenolphthalein (FDA 02/25/19)
- Kingston Pharma, LLC Issues Voluntary Recall of All Lots of DG™ Baby Gripe Water Due to Undissolved Ingredient, Citrus Flavonoid (FDA 02/15/19)
- FTC & FDA issue warning letters to supplement sellers (FDA 02/11/19)
- FTC and FDA Send Warning Letters to Companies Selling Dietary Supplements Claiming to Treat Alzheimer’s Disease and Remediate or Cure Other Serious Illnesses Such as Parkinson’s, Heart Disease, and Cancer (FDA 02/11/19)
- Nature’s Rx Issues Voluntary Nationwide Recall of Silver Bullet 10x to Undeclared PDE-5 Inhibitors in the Product (FDA 01/29/19)
- Public Notification: GoLean Detox contains hidden drug ingredients (FDA 01/28/19)
- Happy Together, Inc. Issues Voluntary Nationwide Recall of Product Due to Presence of Undeclared Sildenafil and Tadalafil (FDA 01/08/19)
2018
- Fat Burners Zone Issues Voluntary Nationwide Recall of Zero Xtreme Due to Presence of Undeclared Sibutramine (FDA 10/15/18)
- Sprayology Issues Voluntary Nationwide Recall of Homeopathic Aqueous-Based Medicines Due to Microbial Contamination (FDA 10/11/18)
- FDA alerts consumers not to use products distributed by Years to Your Health (FDA 09/14/18)
- BioLyte Laboratories Issues Voluntary Nationwide Recall Due to the Voluntary Nationwide Recall initiated by King Bio Inc. (a Raw Material Supplier) for NeoRelief for Muscle Cramping and Restlessness Topical Gel Due to Possible Microbial Contamination (FDA 09/12/18)
- Beaumont Bio Med, Inc. Issues Voluntary Nationwide Recall of all their Homeopathic Aqueous/Alcohol-Based Medicines due to the Nationwide Recall by the Contract Manufacturer, King Bio, of all their Aqueous-Based Products-Possible Microbial Contamination (FDA 09/05/18)
- Hellolife, Inc. Issues Voluntary Worldwide Recall of Neuroveen, Respitrol, Thyroveev and Compulsin due to Possible Microbial Contamination (FDA 08/29/18)
- Living Well Remedies, LLC Issues Voluntary Nationwide Recall of Weight Away Remedy, Lot # 111417LWL614, Due To Microbial Contamination (FDA 08/24/18)