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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.

2019

Sheaya Lender contains hidden drug ingredients (FDA)
September 6, 2019

Love in S contains hidden drug ingredients (FDA)
September 6, 2019

Mero Macho contains hidden drug ingredient (FDA)
September 6, 2019

LOBO contains hidden drug ingredient (FDA)
September 6, 2019

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)
September 3, 2019

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)
August 29, 2019

FTC Refunds Consumers Who Bought FlexiPrin Joint Pain Supplement (FDA)
August 22, 2019

FDA warns consumers about the dangerous and potentially life threating side effects of Miracle Mineral Solution (FDA)
August 12, 2019

FDA warns company marketing unapproved cannabidiol products with unsubstantiated claims to treat cancer, Alzheimer’s disease, opioid withdrawal, pain and pet anxiety (FDA)
July 23, 2019

Public Notification: Big Penis contains hidden drug ingredient (FDA)
July 16, 2019

DaVinci Laboratories Issues Allergy Alert on Undeclared Fish Allergen in Omega-3 1000 Product Lot 35532200 (FDA)
July 11, 2019

Statement on warning for women of childbearing age about possible safety risks of dietary supplements containing vinpocetine (FDA)
June 3, 2019

STIFF BOY LLC. Issues Voluntary Nationwide Recall of THE BEAST Capsules Due to Presence of Undeclared Sildenafil (FDA)
May 8, 2019

Geniux Dietary Supplement Sellers Barred from Unsupported Cognitive Improvement Claims (FDA)
April 10, 2019

SD Import Issues Voluntary Nationwide Recall of Aphrodisiac Capsules Due to Presence of Undeclared Sildenafil (FDA)
April 9, 2019

Sunstone Organics Issues Voluntary Nationwide Recall of Select Kratom Products Due to Potential Contamination by Salmonella (FDA)
March 1, 2019

Kingston Pharma, LLC Issues Voluntary Recall of All Lots of DG™ Baby Gripe Water Due to Undissolved Ingredient, Citrus Flavonoid (FDA)
February 15, 2019

FTC & FDA issue warning letters to supplement sellers (FDA)
February 11, 2019

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)
February 11, 2019

Happy Together, Inc. Issues Voluntary Nationwide Recall of Product Due to Presence of Undeclared Sildenafil and Tadalafil (FDA)
January 8, 2019

2018

Fat Burners Zone Issues Voluntary Nationwide Recall of Zero Xtreme Due to Presence of Undeclared Sibutramine (FDA)
October 15, 2018

Sprayology Issues Voluntary Nationwide Recall of Homeopathic Aqueous-Based Medicines Due to Microbial Contamination (FDA)
October 11, 2018

FDA alerts consumers not to use products distributed by Years to Your Health (FDA)
September 14, 2018

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)
September 12, 2018

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)
September 5, 2018