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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.

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

Badger Botanicals Recalls Red Suma, Green Suma, Green Hulu 2, And Red Hulu 2 Kratom Supplements Because Of Possible Salmonella Health Risk (FDA)
May 4, 2018

Nutrizone Recalls Various Lots of Multiple Dietary Supplements Because of Possible Salmonella Health Risk (FDA)
April 18, 2018

Viable Solutions, LLC Recalls Certain Kratom-Containing Powder Products Because of Possible Health Risk (FDA)
April 17, 2018

Epic Products, LLC, Issues Voluntary Nationwide Recall of All Lots of Euphoric Capsules Due to Presence of Undeclared Sildenafil and Tadalafil (FDA)
April 16, 2018

'Rhino 69 Extreme 50000' Recalled due to Presence of Active Ingredient 'Tadalafil' (FDA)
April 12, 2018

Club 13 Recalls Kratom Maeng Da Red Powder and Capsules Because of Possible Health Risk (FDA)
April 5, 2018

FTC Sending Refund Checks Totaling More Than $355,000 to Consumers Who Bought CogniPrin ‘Memory Improvement’ Supplement (FDA)
April 2, 2018

Tamarack Inc. Recalls Eclipse Kratom Because of Possible Salmonella Contamination (FDA)
March 23, 2018

PDX Aromatics Issues Second Expanded Recall of Kratom Products Because of Possible Health Risk (FDA)
March 22, 2018

PDX Aromatics Recalls Kratom Powder Because Of Possible Health Risk (FDA)
March 10, 2018

FDA Investigates Multistate Outbreak of Salmonella Infections Linked to Products Reported to Contain Kratom (FDA)
February 20, 2018

Statement from FDA Commissioner Scott Gottlieb, M.D., on the agency’s scientific evidence on the presence of opioid compounds in kratom, underscoring its potential for abuse (FDA)
February 6, 2018

Bulletproof 360, Inc. Issues Allergy Alert on Undeclared Milk in Collagen Protein Dietary Supplement (FDA)
January 25, 2018

FTC, FDA Warn Companies about Marketing and Selling Opioid Cessation Products (FTC)
January 24, 2018

Break Ventures/California Basics Recalls "Zero For Him" 150ct Lot#1710-638 Because of Possible Health Risk (FDA)
January 24, 2018

Flawless Beauty, LLC Issues Voluntary Recall of Unapproved Drugs (FDA)
January 19, 2018

2017

FTC Sending Refund Checks Totaling More Than $8 Million to Consumers Who Bought Deceptively Marketed Weight-loss Supplements (FDA)
December 6, 2017

Supplement Sellers Settle FTC, State of Maine False Advertising Charges (FTC)
November 30, 2017