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

1,464 recalls · Class II, newest first

Class II · Moderate risk

5% Dextrose Injection

Lack of Assurance of Sterility. Complaints were receive of missing closures and/or leaks which may compromise product sterility.

Terminated Sterility / contamination Baxter Healthcare Corp. NDC 0338-0017-04 D-0426-2015
Class II · Moderate risk

0.9% Sodium Chloride Injection

Lack of Assurance of Sterility. Complaints were receive of missing closures and/or leaks which may compromise product sterility.

Terminated Sterility / contamination Baxter Healthcare Corp. NDC 0338-0049-03 D-0425-2015
Class II · Moderate risk

Captopril Tablets

Failed Tablet/Capsule Specifications: out of specification for thickness.

Terminated Failed specification Wockhardt Usa Inc. NDC 64679-902-01 D-0975-2015
Class II · Moderate risk

Domperidone BP

Penicillin Cross Contamination: Potential for products to be cross-contaminated with penicillin.

Terminated Cross-contamination Freedom Pharmaceuticals Inc D-0567-2016
Class II · Moderate risk

Ergoloid Mesylates

Failed Impurities/Degradation Specifications: during long-term stability testing.

Terminated Impurity / degradation Mutual Pharmaceutical Company, Inc. NDC 53489-281-01 D-0414-2015
Class II · Moderate risk

Triest 80/10/10

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0228-2016
Class II · Moderate risk

Triest 80/10/10

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0227-2016
Class II · Moderate risk

Triest 70/20/10

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0226-2016
Class II · Moderate risk

Estriol 5 Estradiol

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

Terminated Cross-contamination the Compounder D-0225-2016

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