HIGHFDA DRUG
Westminster Pharmaceuticals Recalls Metoprolol Tartrate Tablets Due to Nitrosamine Contamination
Westminster Pharmaceuticals recalled 16,672 bottles of Metoprolol Tartrate Tablets on August 6, 2025. The recall stems from high levels of a harmful nitrosamine, N-nitroso-metoprolol, exceeding the Acceptable Daily Intake. Consumers must stop using the tablets immediately and consult healthcare providers for guidance.
METOPROLOL TARTRATE
CGMP Deviations: