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

832 recalls, newest first

Class II · Moderate risk

Sensorcaine-MPF

Subpotent Drug: Low out-of-specification assay results for the epinephrine component.

Terminated Wrong potency / content Fresenius Kabi USA, LLC NDC 63323-462-01 D-0172-2021
Class II · Moderate risk

Hydroxyzine Hydrochloride Oral Solution

Failed Impurities/Degradation Specification: OOS for the following - unknown degradant/impurity, 4-chorobenzophenone, and for total impurities.

Terminated Impurity / degradation Morton Grove Pharmaceuticals, Inc. NDC 60432-150-04 D-0174-2021
Class II · Moderate risk

Vumerity (diroximel fumarate)

Failed dissolution specifications: out-of-specification test results observed during the buffer stage dissolution testing.

Terminated Dissolution failure Biogen MA Inc. NDC 64406-020-01 D-0148-2021
Class II · Moderate risk

Sodium Chloride Injection

Failed pH Specifications: Out of Specification pH Test Results were found in Sodium Chloride Injection USP 0.9% 2ml vial.

Terminated Failed specification Hikma Pharmaceuticals USA Inc. NDC 0641-0497-17 D-0169-2021
Class II · Moderate risk

Sildenafil Tablets USP 100 mg

Product mix-up: Bottles of sildenafil and trazodone were inadvertently packaged together during bottling at a 3rd party facility.

Terminated Chemical / undeclared AVKARE Inc. NDC 42291-748-01 D-0167-2021

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