Metoprolol is a beta blocker used for high blood pressure and heart conditions. We track every FDA enforcement recall involving Metoprolol (Lopressor, Toprol) — 23 recalls in our database, including 8 active.
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Teva Pharmaceuticals USA, Inc — Failed Dissolution Specifications
Recall D-0354-2026
Teva Pharmaceuticals USA, Inc — Failed Dissolution Specifications
Recall D-0356-2026
Teva Pharmaceuticals USA, Inc — Failed Dissolution Specifications
Recall D-0357-2026
Teva Pharmaceuticals USA, Inc — Failed Dissolution Specifications
Recall D-0355-2026
Westminster Pharmaceuticals LLC — CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the established Acceptable Daily Intake (ADI) level.
Recall D-0582-2025
Westminster Pharmaceuticals LLC — CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the established Acceptable Daily Intake (ADI) level.
Recall D-0581-2025
Granules Pharmaceuticals Inc. — Failed Dissolution Specifications: Product failed to meet dissolution acceptance criteria in the stability studies at the 6th month (25¿C/60% RH) long-term.
Recall D-0510-2025
Rubicon Research Private Limited — Presence of Foreign Substance: metal in tablet
Recall D-0517-2024
Showing 8 of 23. See all Metoprolol recalls.
This page is for information only and isn’t medical advice. Always follow your clinician’s guidance.
The FDA publishes recalls, but most never make the news. The reliable way is an automated alert: sign up free and we’ll email you when a Metoprolol recall is issued.
Most prescriptions filled in the US are generics, so most recalls involve generic products. A recall doesn’t mean the drug itself is unsafe — it usually affects specific lots or manufacturers.
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