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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.

Rhinozen 69 Platinum 25000 contains hidden drug ingredient (FDA)
November 24, 2020

Rhino 99 Extreme 90000 contains hidden drug ingredient (FDA)
November 24, 2020

Stree Overlord contains hidden drug ingredients (FDA)
November 24, 2020

U.S.A Viagra contains hidden drug ingredient (FDA)
November 24, 2020

V8 Super Energy contains hidden drug ingredient (FDA)
November 24, 2020

Fusion Health and Vitality Issues Voluntary Nationwide Recall of Core Essential Nutrients and Immune Boost Sublingual Vitamin D3 Due to the Unapproved Use of a Food Additive and Unapproved Marketing Statements (FDA)
November 23, 2020

FTC Approves Administrative Complaint Against Supplement Marketer Health Research Laboratories, LLC (FTC)
November 20, 2020

FTC Sends Letters Warning 20 More Marketers to Stop Making Unsupported Claims That Their Products and Therapies Can Effectively Prevent or Treat COVID-19 (FTC)
November 12, 2020

FTC Approves Final Administrative Consent Order with Marketer of Product Falsely Claiming to Prevent or Treat COVID-19 (FTC)
October 19, 2020

Do Not Use: Black Salve is Dangerous and Called by Many Names (FDA)
October 13, 2020

FDA Warns Dietary Supplement Companies Illegally Selling Products Containing Cesium Chloride (FDA)
October 13, 2020

FTC Refunds More Than $76,000 to Consumers Who Bought Deceptively Marketed “Miracle” Pain Cure for Older Adults (FTC)
September 24, 2020

RLC Labs, Inc., Issues Voluntary Nationwide Recall of All Lots of Nature-Throid® and WP Thyroid® with Current Expiry Due to Sub Potency (FDA)
September 3, 2020

The Protein Shoppe, LLC Issues Voluntary Nationwide Recall of the “Red- E” Male Enhancement Tablet Due to the Presence of Undeclared Sildenafil (FDA)
September 1, 2020

FDA advises consumers not to use goldenseal root power distributed by Maison Terre (FDA)
August 14, 2020

Summitt Labs Issues Voluntary Nationwide Recall of KORE ORGANIC Watermelon CBD Oil Due to High Lead Results (FDA)
July 28, 2020

FTC Order Stops the Marketer of “Thrive” Supplement from Making Baseless Claims It Can Treat, Prevent, or Reduce the Risks from COVID-19 (FTC)
July 10, 2020

Sundial Herbal Products is Recalling Products Attached Because these Products were Misbranded. The Products are Currently Unapproved Drugs, Recall is Required by the Order
July 9, 2020

FTC Sends Letters Warning 30 More Marketers to Stop Making Unsupported Claims That Their Products and Therapies Can Effectively Prevent or Treat COVID-19 (FTC)
June 18, 2020

FDA Warns Four Manufacturers of Unapproved Injectable Drugs Labeled as Homeopathic (FDA)
June 16, 2020

GSK Consumer Healthcare Recalls Benefiber Healthy Shape Prebiotic Fiber Supplement and Benefiber Prebiotic Fiber Supplement Due to Possible Plastic Contamination from the Bottle Cap (FDA)
May 28, 2020

StayWell Copper Products (FDA)
May 28, 2020

FTC Sending Refund Checks Totaling More Than $470,000 to Consumers Defrauded by Misleading Health Claims for TrueAloe and AloeCran Supplements (FTC)
May 26, 2020

FTC Sends Letters Warning 50 More Marketers to Stop Making Unsupported Claims That Their Products and Therapies Can Effectively Prevent or Treat COVID-19 (FTC)
May 21, 2020

Biota Biosciences Issues Voluntary Nationwide Recall of Cannabidiol (CBD) Complex, Curcumin Complex, and Cannabidiol + Curcumin Injectables Because They Were Marketed Without FDA Approval (FDA)
May 20, 2020