Independent register of U.S. FDA drug recalls · updated Oct 11, 2026
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FDA Drug Recalls

18,003 recalls, newest first

Class III · Low risk

Fluconazole Injection

Superpotent Drug: lots out of specification for elevated sodium chloride and fluconazole assay.

Terminated Wrong potency / content Renaissance Lakewood, LLC D-1033-2018
Class III · Low risk

Fluconazole Injection

Failed Stability Specifications: lot out of specification for elevated water vapor.

Terminated Stability / shelf life Renaissance Lakewood, LLC NDC 36000-002-10 D-1032-2018
Class III · Low risk

Fluconazole Injection

Superpotent Drug and Failed Stability Specifications: lot out of specification for elevated sodium chloride and elevated water vapor.

Terminated Wrong potency / content Renaissance Lakewood, LLC NDC 36000-003-06 D-1031-2018
Class III · Low risk

Diazepam Rectal Gel

Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed without a lot number or expiration date on the outer carton.

Terminated Labeling / mix-up Valeant Pharmaceuticals North America LLC NDC 68682-650-20 D-1041-2018
Class II · Moderate risk

Admelog Solostar

Temperature Abuse: Product samples of Admelog may not have been shipped at proper temperature.

Ongoing Temperature excursion Sanofi-Aventis U.S. LLC NDC 0024-5925-00 D-0925-2018
Class II · Moderate risk

Fluocinolone Acetonide Topical Solution

Failed Impurities and Degradation Specifications and Subpotent Drug: out-of-specification (OOS) test results for below assay and above specification for degradants.

Terminated Impurity / degradation Teva Pharmaceuticals USA NDC 0591-2990-60 D-0909-2018
Class II · Moderate risk

Metformin Hydrochloride Extended Release Tablets

Presence of foreign substance: One lot fo Metformin Hydrochloride Extended Release Tablets, USP, 500 mg (500 Count) contains foreign matter identified as a piece of rubber glove detected in one tablet.

Terminated Particulate / foreign matter Sun Pharmaceutical Industries, Inc. NDC 62756-142-02 D-0924-2018
Class II · Moderate risk

Monsel's Solution

CGMP Deviations: The manufacturer of this product recalled because they were not manufactured under current good manufacturing practices.

Terminated cGMP deviation Medgyn Products, Inc. NDC 42721-112-08 D-0917-2018
Class I · High risk

Neostigmine Methylsulfate Injection Solution

Labeling: Label Error on Declared Strength: syringes of Neostigmine Methylsulfate 1 mg per mL, 5 mg per 5 mL may be incorrectly labeled as Neostigmine Methylsulfate 1 mg per mL, 3 mg per 3 mL.

Terminated Labeling / mix-up Fagron Compounding Services LLC dba Fagron Sterile Services NDC 71266-2003-01 D-0911-2018
Class I · High risk

Neostigmine Methylsulfate Injection Solution

Labeling: Label Error on Declared Strength: syringes of Neostigmine Methylsulfate 1 mg per mL, 5 mg per 5 mL may be incorrectly labeled as Neostigmine Methylsulfate 1 mg per mL, 3 mg per 3 mL.

Terminated Labeling / mix-up Fagron Compounding Services LLC dba Fagron Sterile Services NDC 71266-2003-02 D-0910-2018
Class II · Moderate risk

Daptomycin for Injection

Microbial Contamination of Sterile Products: Product associated with reports of adverse events indicative of infusion reactions related to microbiological contamination.

Terminated Microbial contamination Pfizer NDC 0409-0106-01 D-1023-2018
Class III · Low risk

Enalapril Maleate

Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.

Terminated Impurity / degradation Aidarex Pharmaceuticals LLC D-0992-2018
Class III · Low risk

Enalapril Maleate

Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.

Terminated Impurity / degradation Aidarex Pharmaceuticals LLC D-0991-2018
Class III · Low risk

Enalapril Maleate

Out-of-specification results for the Enalapril Diketopiperazine degradation product during commercial stability.

Terminated Impurity / degradation Aidarex Pharmaceuticals LLC D-0990-2018

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