Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA drug recalls in 2022

Every FDA drug recall initiated in 2022, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.

1,390 recalls, newest first.

Class II · Moderate risk

Back Pain-Off

cGMP deviations

Terminated cGMP deviation Ultra Seal Corporation NDC 47682-073-00 D-0476-2022
Class II · Moderate risk

Ephedrine Plus

cGMP deviations

Terminated cGMP deviation Ultra Seal Corporation NDC 65193-320-24 D-0473-2022
Class II · Moderate risk

Chloresin

cGMP deviations

Terminated cGMP deviation Ultra Seal Corporation NDC 51532-0107-2 D-0468-2022
Class II · Moderate risk

Proctofoam HC

cGMP deficiencies

Terminated cGMP deviation Mylan Pharmaceuticals Inc NDC 0037-6822-10 D-0452-2022
Class III · Low risk

Bortezomib

Failed stability specifications

Terminated Stability / shelf life Dr. Reddy's Laboratories, Inc. NDC 43598-865-60 D-0577-2022
Class III · Low risk

Azacitidine

Failed stability specifications

Terminated Stability / shelf life Dr. Reddy's Laboratories, Inc. NDC 43598-465-62 D-0576-2022
Class III · Low risk

Azacitidine

Failed stability specifications

Terminated Stability / shelf life Dr. Reddy's Laboratories, Inc. NDC 43598-305-62 D-0575-2022
Class II · Moderate risk

Lexette (halobetasol propionate)

CGMP Deviation: Difficulty dispensing/does not dispense or dispensing liquid instead of foam.

Ongoing cGMP deviation Mayne Pharma Inc NDC 51862-604-50 D-0387-2022
Class II · Moderate risk

Tretinoin Capsules

Failed Dissolution Specifications; Low Out of specification (OOS) results for dissolution.

Terminated Dissolution failure Teva Pharmaceuticals USA NDC 0555-0808-02 D-0520-2022

Recalls by year