U.S. flag An official website of the United States government

On Oct. 1, 2024, the FDA began implementing a reorganization impacting many parts of the agency. We are in the process of updating FDA.gov content to reflect these changes.

U.S. Food and Drug Administration
  1. Home
  2. Drugs
  3. Drug Safety and Availability
  4. Drug Recalls
  1. Drug Safety and Availability

Drug Recalls

A drug recall is the most effective way to protect the public from a defective or potentially harmful product. A recall is a voluntary action taken by a company to remove a defective drug product from the market or warn patients and consumers about a potential risk.

The list below includes voluntary drug recalls in which public notification has been issued.

Visit FDA’s role in drug recalls for more information.
Visit Recalls, Market Withdrawals, & Safety Alerts for all FDA-regulated products.
Follow FDA Recall Information on X (formerly Twitter).



Filter by

A Terminated Recall is a recall where the FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard. Recalls that are not indicated as being terminated are either ongoing or completed.

Date Brand Name(s) Product Description Recall Reason Description Company Name Terminated Recall Excerpt
Par Pharmaceutical Adrenalin® Chloride Solution (EPINEPHrine nasal solution, USP) Product is an unapproved drug. Endo, Inc.
Fouzee SugarLin Herbal Formula Herbal Dietary Supplement Product contains undeclared Metformin and Glyburide Shoppers-Plaza
Force Forever Dietary Supplement Product contains undeclared diclofenac and dexamethasone GNMART Inc
Buy-herbal.com Nhan Sam Tuyet Lien Truy Phong Hoan dietary supplement capsules Device & Drug Safety – Unapproved Drug Buy-herbal.com
Umary UMARY Hyaluronic Acid tablets The product contains undeclared diclofenac and omeprazole MXBBB
Par Pharmaceutical Clonazepam Orally Disintegrating Tablets, USP (C-IV) Mislabeled with the incorrect strength on the carton Endo, Inc.
VitalityVita Marketed as Dietary Supplement Undeclared Sildenafil and Diclofenac VitalityVita
Boulla LLC Marketed as Dietary Supplement Undeclared Sildenafil and Diclofenac Boulla LLC
AK Forte AK Forte Dietary Supplement Device & Drug Safety – Unapproved Drug C&A Naturistics
STASKA Pharmaceuticals Ascorbic Acid Solution for Injection Device & Drug Safety – Presence of glass particulates STASKA Pharmaceuticals Inc.
Download XLSX
Back to Top