Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA drug recalls in 2025

Every FDA drug recall initiated in 2025, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.

778 recalls, newest first.

Class II · Moderate risk

LIDOcaine HCl Injection

Lack of Assurance of Sterility: A recent FDA inspection revealed concerns with the sterile manufacturing process.

Ongoing Sterility / contamination Tailstorm Health INC NDC 81483-0000-0 D-0498-2025
Class II · Moderate risk

Testo-200

Marketed Without an Approved NDA/ANDA

Ongoing Unapproved drug Advanced Pharmaceutical Technology, Inc. NDC 57377-200-01 D-0531-2025
Class II · Moderate risk

Icosapent Ethyl Capsules 1 gram

Failed Tablet/Capsule specifications; a product complaint was reported for burnt or melted capsules. This was determined to be a result of oxidation by leakage of capsule contents.

Completed Failed specification Zydus Pharmaceuticals (USA) Inc NDC 70710-1592-7 D-0497-2025
Class II · Moderate risk

Gentamicin Injection

Failed Stability Specifications: Out of specification results for the Color Absorbance test during 12 Month sample analysis.

Ongoing Stability / shelf life Eugia US LLC NDC 55150-401-01 D-0472-2025
Class II · Moderate risk

Lacosamide Oral Solution

Defective Container: This recall is being initiated due to a leaking unit stored horizontally.

Ongoing Packaging defect Apotex Corp. NDC 60505-0405-4 D-0457-2025
Class II · Moderate risk

Fluoxetine Tablets

CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim acceptable intake limit.

Completed Nitrosamine impurity Torrent Pharma Inc. D-0456-2025
Class II · Moderate risk

Fluoxetine Tablets

CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim acceptable intake limit.

Completed Nitrosamine impurity Torrent Pharma Inc. D-0455-2025
Class II · Moderate risk

Cephalexin for Oral Suspension

Failed Impurities/Degradation Specifications An out-of-specification result was observed in the related substance test at the sixth month of stability analysis. The individual impurity was identified to be Cephalexin Glucose Adduct.

Ongoing Impurity / degradation Ascend Laboratories, LLC NDC 67877-544-68 D-0469-2025
Class II · Moderate risk

Cephalexin for Oral Suspension

Failed Impurities/Degradation Specifications An out-of-specification result was observed in the related substance test at the sixth month of stability analysis. The individual impurity was identified to be Cephalexin Glucose Adduct.

Ongoing Impurity / degradation Ascend Laboratories, LLC NDC 67877-544-88 D-0468-2025
Class II · Moderate risk

Acetaminophen Tablets

cGMP deviations: Due to confirmed consumer complaints received with the observation of tablet discoloration (brown surface on tablets).

Ongoing Failed specification Aurobindo Pharma USA Inc NDC 72288-405-10 D-0471-2025
Class I · High risk

Umovy Acido Hialuronico

Marketed without approved NDA/ANDA- Laboratory analysis found product to be tainted with undeclared ingredients: Dexamethasone and Diclofenac.

Completed Chemical / undeclared Umary-USA.com D-0493-2025
Class I · High risk

Unavy Acido Hialuronico

Marketed without approved NDA/ANDA- Laboratory analysis found product to be tainted with undeclared ingredients: Dexamethasone, Diclofenac and Omeprazole.

Completed Chemical / undeclared Umary-USA.com D-0492-2025

Recalls by year