Alerts and Advisories

• 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

• 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