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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.

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

Hellolife, Inc. Issues Voluntary Worldwide Recall of Neuroveen, Respitrol, Thyroveev and Compulsin due to Possible Microbial Contamination (FDA)
August 29, 2018

Living Well Remedies, LLC Issues Voluntary Nationwide Recall of Weight Away Remedy, Lot # 111417LWL614, Due To Microbial Contamination (FDA)
August 24, 2018

King Bio Issues Voluntary Nationwide Recall of It’s Kids and Infant Products Due to Potential Microbial Contamination (FDA)
August 22, 2018

Zakah Life Recalls Kratom Because Of Possible Health Risk (FDA)
August 14, 2018

World Organix, LLC Issues Voluntary Nationwide Recall of Blissful Remedies Red Maeng Da 100% Mitragyna Speciosa, Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa, Blissful Remedies 4 Hour Chill Slow Motion Blend, Due to High Microbial Loads (FDA)
August 13, 2018

King Bio Issues Voluntary Nationwide Recall of Aquaflora Candida HP9, Lymph Detox, and Baby Teething Liquids Due to Microbial Contamination (FDA)
July 20, 2018

LL’S Magnetic Clay Inc. Expands Allergy Alert On Undeclared Allergens In Prescript-Assist Dietary Supplement To All Lots (FDA)
July 6, 2018

Blissful Remedies Issues Voluntary Nationwide Recall of Certain Kratom Powder Capsule (FDA)
June 30, 2018

FDA warns companies selling illegal, unapproved kratom products marketed for opioid cessation, pain treatment and other medical uses (FDA)
May 22, 2018

Shoreside Enterprises Issues Voluntary Nationwide Recall of 7K and Poseidon 4500 (Extreme 1000 Mg) Due to Presence of Undeclared Sildenafil and Tadalafil (FDA)
May 17, 2018