Alerts and Advisories

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