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
- Fat Burners Zone Issues Voluntary Nationwide Recall of Zero Xtreme Due to Presence of Undeclared Sibutramine (FDA 10/15/18)
- Sprayology Issues Voluntary Nationwide Recall of Homeopathic Aqueous-Based Medicines Due to Microbial Contamination (FDA 10/11/18)
- FDA alerts consumers not to use products distributed by Years to Your Health (FDA 09/14/18)
- 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 09/12/18)
- 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 09/05/18)
- Hellolife, Inc. Issues Voluntary Worldwide Recall of Neuroveen, Respitrol, Thyroveev and Compulsin due to Possible Microbial Contamination (FDA 08/29/18)
- Living Well Remedies, LLC Issues Voluntary Nationwide Recall of Weight Away Remedy, Lot # 111417LWL614, Due To Microbial Contamination (FDA 08/24/18)
- King Bio Issues Voluntary Nationwide Recall of It’s Kids and Infant Products Due to Potential Microbial Contamination (FDA 08/22/18)
- Zakah Life Recalls Kratom Because Of Possible Health Risk (FDA 08/14/18)
- 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 08/13/18)
- King Bio Issues Voluntary Nationwide Recall of Aquaflora Candida HP9, Lymph Detox, and Baby Teething Liquids Due to Microbial Contamination (FDA 07/20/18)
- LL’S Magnetic Clay Inc. Expands Allergy Alert On Undeclared Allergens In Prescript-Assist Dietary Supplement To All Lots (FDA 07/06/18)
- Blissful Remedies Issues Voluntary Nationwide Recall of Certain Kratom Powder Capsule (FDA 06/30/18)
- Shoreside Enterprises Issues Voluntary Nationwide Recall of 7K and Poseidon 4500 (Extreme 1000 Mg) Due to Presence of Undeclared Sildenafil and Tadalafil (FDA 05/17/18)
- Badger Botanicals Recalls Red Suma, Green Suma, Green Hulu 2, And Red Hulu 2 Kratom Supplements Because Of Possible Salmonella Health Risk (FDA 05/04/18)
- NxtGen Botanicals Maeng Da Kratom by NGB Corp.: Recall - Possible Salmonella Contamination (FDA 04/19/18)
- Certain Kratom-Containing Powder Products by Viable Solutions: Recall -Possible Salmonella Contamination (FDA 04/19/18)
- Nutrizone Recalls Various Lots of Multiple Dietary Supplements Because of Possible Salmonella Health Risk (FDA 04/18/18)
- Viable Solutions, LLC Recalls Certain Kratom-Containing Powder Products Because of Possible Health Risk (FDA 04/17/18)
- Epic Products, LLC, Issues Voluntary Nationwide Recall of All Lots of Euphoric Capsules Due to Presence of Undeclared Sildenafil and Tadalafil (FDA 04/16/18)
- 'Rhino 69 Extreme 50000' Recalled due to Presence of Active Ingredient 'Tadalafil' (FDA 04/12/18)
- Maeng Da Red Powder and Capsules by Club 13: Recall - Possible Contamination With Salmonella (FDA 04/10/18)
- Advocare Issues Allergy Alert in Select Bottles of Muscle Strength and Nighttime Recovery Product Because of Undeclared Milk Allergen on The Label (FDA 04/06/18)
- Club 13 Recalls Kratom Maeng Da Red Powder and Capsules Because of Possible Health Risk (FDA 04/05/18)
- Independent Nutrition, Inc Issues Allergy Alert On Undeclared Milk in Ignite Pre-Workout Supplement Products (FDA 04/05/18)
- Kratom-containing Products by Triangle Pharmanaturals: Mandatory Recall - Risk of Salmonella (FDA 04/03/18)
- Dietary Supplements by Nutrizone: Recall - Potential for Salmonella Contamination (FDA 04/03/18)
- FTC Sending Refund Checks Totaling More Than $355,000 to Consumers Who Bought CogniPrin ‘Memory Improvement’ Supplement (FDA 04/02/18)
- Tamarack Inc. Recalls Eclipse Kratom Because of Possible Salmonella Contamination (FDA 03/23/18)
- PDX Aromatics Issues Second Expanded Recall of Kratom Products Because of Possible Health Risk (FDA 03/22/18)
- PDX Aromatics Recalls Kratom Powder Because Of Possible Health Risk (FDA 03/10/18)
- FDA Investigates Multistate Outbreak of Salmonella Infections Linked to Products Reported to Contain Kratom (FDA 02/20/18)
- 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 02/06/18)
- Bulletproof 360, Inc. Issues Allergy Alert on Undeclared Milk in Collagen Protein Dietary Supplement (FDA 01/25/18)
- Break Ventures/California Basics Recalls "Zero For Him" 150ct Lot#1710-638 Because of Possible Health Risk (FDA 01/24/18)
- FTC, FDA Warn Companies about Marketing and Selling Opioid Cessation Products (FTC 01/24/18)
- Flawless Beauty, LLC Issues Voluntary Recall of Unapproved Drugs (FDA 01/19/18)
2017
- FTC Sending Refund Checks Totaling More Than $8 Million to Consumers Who Bought Deceptively Marketed Weight-loss Supplements (FDA 12/06/17)
- Supplement Sellers Settle FTC, State of Maine False Advertising Charges (FTC 11/30/17)
- Florida-based Supplement Sellers Settle FTC False Advertising Charges (FTC 11/20/17)
- Internet Marketers of Dietary Supplement and Skincare Products Banned from Deceptive Advertising and Billing Practices (FTC 11/15/17)
- Statement from FDA Commissioner Scott Gottlieb, M.D. on FDA advisory about deadly risks associated with kratom (FDA 11/14/17)
- Ridge Properties DBA Pain Relief Naturally Issues Voluntary Nationwide Recall of all lots of Naturally HL Bedsore Cream, Pretat by TAT Balm Carbomer Free Gel, & All Naturally HL Hemorrhoid products due to manufacturing concerns at the facility (FDA 11/01/17)
- U.S. District Court Rules in FTC’s Favor, Imposes $40 Million Judgment Against Weight-Loss Supplement Marketers for Order Violations (FTC 10/16/17)
- FTC Sending Refund Checks Totaling More Than $9.8 Million to People Who Were Charged for “Free Trials” for Health Products (FDA 10/10/17)
- Kiriko, LLC. Issues Voluntary Nationwide Recall of A1 Slim Due to Undeclared Sibutramine, Phenolphthalein and N-Desmethyl sibutramine (FDA 10/05/17)
- Gadget Island, Inc. dba Gear Isle Issues Voluntary Nationwide Recall of Rhino 7 Platinum 5000, Papa Zen 3300, Fifty Shades 6000 and Grande X 5800, Due to Presence of Undeclared Sildenafil, Tadalafil and Desmethyl Carbodenafil (FDA 10/04/17)
- FTC Sending Refund Checks Totaling More Than $210,000 to Consumers Who Bought Elimidrol ‘Opiate Withdrawal’ Product (FTC 09/28/17)
- Physic Candy – Define contains hidden drug ingredients (FDA 09/11/17)
- Physic Candy – Curve contains hidden drug ingredients (FDA 08/31/17)