Alerts and Advisories

2024

• VitalityVita Issues Voluntary Nationwide Recall of VitalityXtra and PeakMax Capsules Due to the Presence of Undeclared Sildenafil and Diclofenac (FDA)
  November 6, 2024

• Boulla LLC Issues Voluntary Nationwide Recall of ZoomMax and ZapMax Capsules Due to the Presence of Undeclared Sildenafil and Diclofenac (FDA)
  November 5, 2024

• C&A Naturistics Issues Voluntary Nationwide Recall of AK Forte Tablets con Ortiga y Omega 3 Due to the Presence of Undeclared Drug Ingredients: Diclofenac, Dexamethasone, and Methocarbamol
  October 16, 2024

• 123Herbals LLC (123Herbals.com) Issues Voluntary Nationwide Recall of Vail-Bon Jie Yang Wan Capsules Due to the Presence of Undeclared Dexamethasone and Chlorpheniramine (FDA)
  September 20, 2024

• Boulla LLC Issues Voluntary Nationwide Recall of Boom Max Capsules Due to the Potential Presence of Undeclared Sildenafil (FDA)
  August 21, 2024

• FDA warns consumers to not purchase or use unapproved inhalant products marketed for alertness and energy boosting (FDA)
  August 6, 2024

• FDA Warns Consumers Not to Use Optimized Plant Mediated Solutions (OPMS) Black Liquid Kratom (FDA)
  July 26, 2024

• GURU INC. Issues Voluntary Nationwide Recall of Infla-650 Herbal Dietary Supplement Capsules Due to Hidden Drug Ingredients (FDA)
  July 16, 2024

• Supercore Products Group, Inc. Issues Voluntary Worldwide Recall of Hard Steel Capsules & Gold Hard Steel Plus Liquid Due to the Presence of Sildenafil and Acetaminophen (FDA)
  July 12, 2024

• Penn Herb Company Ltd Recalls Nature’s Wonderland Thyroid Formula Because of Possible Health Risk (FDA)
  June 12, 2024

• Investigation of Illnesses: Diamond Shruumz-Brand Chocolate Bars, Cones, & Gummies (FDA)
  June 11, 2024

• Male Enhancement Supplements Recalled (FDA)
  June 11, 2024

• Investigation of Illnesses: Diamond Shruumz-Brand Microdosing Chocolate Bars (FDA)
  June 7, 2024

• HomeoCare Laboratories Inc. Issues Voluntary Nationwide Recall of Homeopathic Stella Life Oral Care Spray Unflavored and Advanced Formula Peppermint Oral Care Rinse Due to Microbial Contamination (FDA)
  June 5, 2024

• STOP CLOPEZ CORP Issues Voluntary Worldwide Recall of Schwinnng Capsules Due to the Presence of Undeclared Nortadalafil (FDA)
  April 23, 2024

• Global Mix, Inc Recalls Tejocote Products Because of Possible Health Risk (FDA)
  April 10, 2024

• ForeverMen Supplements Recalled (FDA)
  April 2, 2024

• Pyramid Wholesale Issues Recall of Various Brands of Products Sold as Dietary Supplements for Sexual Enhancement Because They Contain Undeclared Prescription Drugs Including Sildenafil (Viagra) and/or Tadalafil (Cialis) (FDA)
  March 21, 2024

• G.A. Mart Issues Voluntary Nationwide Recall of H&NATURAL TejoRoot and H&NATURAL Brazil Seed Dietary Supplements Due to the Presence of Yellow Oleander (Thevetia peruviana), a Poisonous Plant Native to Mexico and Central America (FDA)
  February 23, 2024

• Backstage Center is Issuing a Recall of Approximately 280 Bottles of Alipotec Raiz de Tejocote, Dietary Supplements, that are Labeled with the "Alipotec King" Sticker (FDA)
  February 23, 2024

• Nordic Naturals Issues Voluntary Recall of Baby's Vitamin D3 Liquid Due to Elevated Levels of Vitamin D3 (FDA)
  February 19, 2024

• Today The World Issues Voluntary Nationwide Recall of All Lots of Arize Herbal Dietary Supplement Capsules Due to the Presence of Undeclared Nortadalafil (FDA)
  February 5, 2024

• FDA Issues Warning About Certain Supplements Substituted with Toxic Yellow Oleander (January 2024) (FDA)
  January 26, 2024

• FDA Warns Consumers Not to Purchase or Use Neptune’s Fix or Any Tianeptine Product Due to Serious Risks (FDA)
  January 23, 2024

• FDA Issues Warning About Certain Tejocote Root Supplements Substituted with Toxic Yellow Oleander (FDA)
  January 5, 2024