Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA Drug Recalls

18,003 recalls, newest first

Class II · Moderate risk

Advil Liqui-Gel Mini 160+20+20 CT

Labeling: Lacks Warning or Rx Legend- Certain lots does not include required safety warning information in the Drug Facts Panel.

Terminated Labeling / mix-up Glaxosmithkline Consumer Healthcare Holdings NDC 0573-1715-59 D-1069-2020
Class II · Moderate risk

*Mitomycin 0.04% Ophth DR eye drops

Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Terminated Sterility / contamination Medical Center Pharmacy, Inc. NDC 67457-0518-05 D-1077-2020
Class II · Moderate risk

*Morphine 2 mg/mL Cassette

Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Terminated Sterility / contamination Medical Center Pharmacy, Inc. NDC 00409-1134-03 D-1075-2020
Class II · Moderate risk

C-*Vancomycin Opthal 14 mg drops

Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Terminated Sterility / contamination Medical Center Pharmacy, Inc. NDC 67457-0340-01 D-1074-2020
Class II · Moderate risk

C-*Albumin Eye Drop 10% S

Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Terminated Sterility / contamination Medical Center Pharmacy, Inc. NDC 44206-0251-05 D-1073-2020
Class II · Moderate risk

Doxycycline Capsules

CGMP Deviations: Doxycycline capsules were not manufactured under Current Good Manufacturing Practice conditions.

Terminated cGMP deviation Sun Pharmaceutical Industries, Inc. NDC 63304-616-50 D-1033-2020
Class II · Moderate risk

Doxycycline Capsules

CGMP Deviations: Doxycycline capsules were not manufactured under Current Good Manufacturing Practice conditions.

Terminated cGMP deviation Sun Pharmaceutical Industries, Inc. NDC 63304-615-01 D-1032-2020
Class III · Low risk

Bekyree

Failed Content Uniformity Specifications: Out Of Specification test results observed for content and blend uniformity.

Terminated Wrong potency / content Lupin Pharmaceuticals Inc. NDC 68180-879-11 D-1055-2020
Class II · Moderate risk

Atorvastatin Calcium Tablets

Presence of foreign substance: Foreign matter has been identified as latex glove in one lot of Atorvastatin Calcium Tablets USP 40 mg.

Terminated Particulate / foreign matter Sun Pharmaceutical Industries, Inc. NDC 63304-829-05 D-1047-2020
Class II · Moderate risk

Theophylline

CGMP Deviations: poor manufacturing practices resulted in Labeling: Incorrect or Missing Lot and/or Exp Date, product incorrectly labeled with incorrect lot and expiration date.

Terminated Stability / shelf life Nostrum Laboratories Inc NDC 29033-001-01 D-1059-2020
Class II · Moderate risk

Epinephrine Injection USP

CGMP Deviations: Precautions taken due to Out-of-specification for trigger force for a non-marketed lot number that shares the same component.

Terminated Failed specification Teva Pharmaceuticals USA NDC 0093-5986-27 D-1260-2020
Class III · Low risk

PrediniSONE Tablets

Labeling: Incorrect or Missing Exp Date - An incorrect expiration date has been identified on Prednisone Tablets USP 5 mg

Terminated Labeling / mix-up Par Pharmaceutical Inc. NDC 0603-5337-31 D-1035-2020

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