Información en Español

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

FDA advises patients not to use Herbal Doctor Remedies’ medicines (FDA)
April 1, 2020

Health Center, Inc. Settles FTC Allegations That It Targeted Older Consumers With Deceptive Claims for Health and Wellness Products (FTC)
March 19, 2020

Mountain Rose Herbs Recalls Organic Kudzu Root Herbal Supplement Due to Possible Health Risk (FDA)
March 18, 2020

Nature Essence Small Molecule Co., LTD (FDA)
March 12, 2020

FTC, FDA Send Warning Letters to Seven Companies about Unsupported Claims that Products Can Treat or Prevent Coronavirus (FTC)
March 9, 2020

FTC: Detox tea claims are hard to swallow (FTC)
March 6, 2020

FTC settles pain relief device case for $4 million (FTC)
March 4, 2020

Med Man Expands Voluntary Nationwide Recall of Up2 and Bow & Arrow Due to Presence of Undeclared Sildenafil (FDA)
February 24, 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: Alpha-Male contains hidden drug ingredients (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

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