Westminster Pharmaceuticals Recalls

2 recalls found for Westminster Pharmaceuticals. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DRUG

Westminster Pharmaceuticals Metoprolol Tartrate 100 mg Recalled for Nitrosamine Above ADI Level (202

Westminster Pharmaceuticals is recalling Metoprolol Tartrate Tablets, 100 mg, 1,000-count bottles distributed nationwide in the United States. The recall concerns CGMP deviations that led to the presence of nitrosamine N-nitroso-metoprolol above the established ADI. Consumers should stop using the product and contact Westminster for guidance.

Metoprolol Tartrate
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Westminster Pharmaceuticals Metoprolol Tartrate 50 mg Recall Over Nitrosamine Above ADI Level (2025)

Westminster Pharmaceuticals recalls 16,672 boxes of Metoprolol Tartrate 50 mg tablets nationwide after nitrosamine exceeds Acceptable Daily Intake. Manufactured by Renata PLC in Bangladesh and distributed in the US by Westminster Pharmaceuticals. Consumers should stop using the product and contact their healthcare provider for guidance.

METOPROLOL TARTRATE
CGMP Deviations:
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Brand Statistics

Total Recalls
2
Pages
1

Related Brands

Metoprolol TartrateMETOPROLOL TARTRATE