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Alerts and Advisories

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

FTC Acts to Stop Two Companies from Making Unproven Bone and Joint Claims (FTC)
February 11, 2020

Public Health Alert Concerning Dietary Supplements Containing Cesium Salts (FDA)
February 5, 2020

FTC Takes Action to Stop Anti-Aging “Cure-All” Marketers From Making Baseless Health Claims (FTC)
February 5, 2020

Public Notification: OrgaZEN Gold 5800 contains hidden drug ingredient (FDA)
February 5, 2020

Public Notification: XXX Platinum WOODIE contains hidden drug ingredients (FDA)
February 5, 2020

Public Notification: RMFLEX contains hidden drug ingredient (FDA)
February 5, 2020

Public Notification: Alpha-Male contains hidden drug ingredients (FDA)
February 5, 2020

Salud Natural Entrepreneur Inc. Recalls Nopalina Flax Seed Fiber Powder and Nopalina Flax Seed Fiber Capsules Because of Possible Health Risk (Updated Lot Number Information) (FDA)
February 3, 2020

Public Health Alert Concerning Nopalina Flax Seed Powder and Nopalina Flax Seed Capsules and Salmonella Contamination (FDA)
January 23, 2020

ABH NATURE’S PRODUCTS, INC, ABH PHARMA, INC., and STOCKNUTRA.COM, INC. Issues Nationwide Recall of All Lots of Dietary Supplement Products (FDA)
January 23, 2020

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)
December 19, 2019

FTC, State of Maine File Contempt Action against Dietary Supplement Marketers (FTC)
December 19, 2019

FTC Sending Additional Refund Checks to Consumers Who Bought LeanSpa Products (FDA)
December 16, 2019

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)
December 11, 2019

FDA warns 15 companies for illegally selling various products containing cannabidiol as agency details safety concerns (FDA)
November 25, 2019

Med Man Issues Voluntary Nationwide Recall of Up2 Due to Presence of Undeclared Sildenafil (FDA)
November 8, 2019

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)
October 22, 2019

JaDera PLUS contains hidden drug ingredients (FDA)
October 6, 2019

Green Lumber contains hidden drug ingredient (FDA)
September 19, 2019

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)
September 16, 2019

FTC Sends Warning Letters to Companies Advertising Their CBD-Infused Products as Treatments for Serious Diseases, Including Cancer, Alzheimer’s, and Multiple Sclerosis (FTC)
September 10, 2019

Anaconda Strong Formula contains hidden drug ingredient (FDA)
September 9, 2019

La Pepa Negra contains hidden drug ingredient (FDA)
September 9, 2019

Lung Leader contains hidden drug ingredient (FDA)
September 9, 2019

Lanugar contains hidden drug ingredients (FDA)
September 6, 2019