Westminster Pharmaceuticals recalls 50mg Metoprolol Tartrate Tablets with nitrosamine levels above safe limits. This medication is prescription-only and may pose health risks if taken.
CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the established Acceptable Daily Intake (ADI) level.
Westminster Pharmaceuticals is recalling 50mg Metoprolol Tartrate Tablets that contain unsafe levels of nitrosamine. These tablets could pose health risks if taken as prescribed.
The tablets contain a nitrosamine compound called N-nitroso-metoprolol at levels above the acceptable daily intake. This chemical could potentially cause health issues when taken as directed by a healthcare provider.
Prescription holders of the recalled Metoprolol Tartrate Tablets, 50mg, 1000 tablets, manufactured by Renata PLC in Bangladesh. Individuals with a prescription for this medication are most at risk.
Check for the product name 'Metoprolol Tartrate Tablets, USP, 50 mg, 1000 Tablets, Rx Only' with the manufacturer Renata PLC (General Plant -2) in Bangladesh. Look for batch numbers R55230021 through R55240121 and expiration dates from September 30, 2025, to July 31, 2026.
Verify the product name, batch number, and expiration date to confirm if your tablets are part of the recall.
The recall indicates the tablets contain nitrosamine levels above safe limits, so they are not safe to take as prescribed.
The recall does not specify a remedy, so contact Westminster Pharmaceuticals for guidance on next steps.
Check for the product name 'Metoprolol Tartrate Tablets, USP, 50 mg, 1000 Tablets, Rx Only' with batch numbers R55230021 through R55240121 and expiration dates from September 30, 2025, to July 31, 2026.
We’ve drafted a message you can send Westminster Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0581-2025 — Westminster Pharmaceuticals Westminster Pharmaceuticals Hello, I own a Westminster Pharmaceuticals that is covered by recall D-0581-2025 from Westminster Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
