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

185 recalls, newest first

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 II · Moderate risk

Monsel's Solution

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Terminated cGMP deviation BioDiagnostic International NDC 42721-112-08 D-0874-2018
Class II · Moderate risk

Loxapine Capsules

CGMP Deviations

Terminated cGMP deviation Mylan Pharmaceuticals Inc. NDC 0378-7050-01 D-0825-2018
Class II · Moderate risk

Loxapine Capsules

CGMP Deviations

Terminated cGMP deviation Mylan Pharmaceuticals Inc. NDC 0378-7025-01 D-0824-2018
Class II · Moderate risk

Amlodipine and Benazapril HCL Capsules

cGMP Deviations; cleaning processes for equipment used to manufacture the specified batches was not followed according to procedure

Terminated cGMP deviation Mylan Pharmaceuticals Inc. NDC 0378-6899-01 D-0820-2018
Class II · Moderate risk

Amlodipine and Benazapril HCL Capsules

cGMP Deviations; cleaning process for equipment used to manufacture the specified batches was not followed according to procedure

Terminated cGMP deviation Mylan Pharmaceuticals Inc. NDC 0378-6896-01 D-0819-2018

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