US Drug Recall Register

FDA Drug Recalls

17,898 recalls, newest first

Class III · Low risk Terminated

Fluconazole Injection

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

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

Diazepam Rectal Gel

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

Valeant Pharmaceuticals North America LLC NDC 68682-650-20 D-1041-2018
Class II · Moderate risk Ongoing

Admelog Solostar

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

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

alba BOTANICA sport mineral sunscreen

Reason Incorrect Product Formulation: wrong sunscreen product in the package.

The Hain Celestial Group, Inc. - Worldwide HQ D-0920-2018
Class II · Moderate risk Terminated

Fluocinolone Acetonide Topical Solution

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

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

Metformin Hydrochloride Extended Release Tablets

Reason 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.

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

Monsel's Solution

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

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

Neostigmine Methylsulfate Injection Solution

Reason 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.

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

Neostigmine Methylsulfate Injection Solution

Reason 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.

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

Daptomycin for Injection

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

Pfizer NDC 0409-0106-01 D-1023-2018
Class II · Moderate risk Terminated

Nitrofurantoin Oral Suspension USP

Reason Subpotent Drug and Failed Content Uniformity.

Lupin Somerset NDC 43386-450-11 D-0927-2018
Class III · Low risk Terminated

Enalapril Maleate

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

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

Enalapril Maleate

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

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

Enalapril Maleate

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

Aidarex Pharmaceuticals LLC D-0990-2018
Class I · High risk Terminated

Blissful Remedies Kratom+CBD CBD infused Maeng Da

Reason Microbial Contamination of Non-Sterile Products: The firm is initiating a recall of some of its products due to the potential of high microbial loads.

World Organix, LLC D-1126-2018
Class I · High risk Terminated

Blissful Remedies Gold Series Ultra Enhanced Indo

Reason Microbial Contamination of Non-Sterile Products: The firm is initiating a recall of some of its products due to the potential of high microbial loads.

World Organix, LLC D-1125-2018
Class I · High risk Terminated

Blissful Remedies

Reason Microbial Contamination of Non-Sterile Products: The firm is initiating a recall of some of its products due to the potential of high microbial loads.

World Organix, LLC D-1123-2018
Class I · High risk Terminated

Blissful Remedies Red Maeng Da

Reason Microbial Contamination of Non-Sterile Products: The firm is initiating a recall of some of its products due to the potential of high microbial loads.

World Organix, LLC D-1122-2018
Class III · Low risk Terminated

Enalapril Maleate Tablets

Reason Failed Impurities/Degradation Specifications: Sub-recall because this repackaged product was recalled by the manufacturing firm, Wockhardt, due to out-of-specification results for the Enalapril DiKetopiperazine degradation product.

Major Pharmaceuticals NDC 0904-5502-61 D-0980-2018
Class III · Low risk Terminated

Enalapril Maleate Tablets

Reason Failed Impurities/Degradation Specifications: Sub-recall because this repackaged product was recalled by the manufacturing firm, Wockhardt, due to out-of-specification results for the Enalapril DiKetopiperazine degradation product.

Major Pharmaceuticals NDC 0904-5609-61 D-0979-2018