Westminster Pharmaceuticals recalls 1000-mg Metoprolol Tartrate Tablets with nitrosamine levels above safe limits. Consumers should check batch numbers for affected lots.
CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the established Acceptable Daily Intake (ADI) level.
Westminster Pharmaceuticals is recalling 1000 Metoprolol Tartrate Tablets (100 mg) that contain a nitrosamine above safe levels. This could pose a health risk with long-term use, but the recall does not specify immediate harm.
The tablets contain a nitrosamine compound (N-nitroso-metoprolol) at levels above the safe daily intake. This chemical is known to be harmful with long-term exposure, but the recall does not indicate immediate danger.
People who have prescription Metoprolol Tartrate Tablets with batch numbers R56240011, R56240021, R56240031, R56240041, R56240051, R56240061, or R56240071. Those with these specific batches are most at risk.
Check the batch number on the tablet packaging. Affected batches are R56240011 (expiring 2/28/26), R56240021/R56240031 (expiring 3/31/26), R56240041/R56240051/R56240061 (expiring 4/30/26), and R56240071 (expiring 7/31/26).
Look for the batch number on the tablet packaging to determine if it is affected.
The recall states the product contains a nitrosamine above safe levels, but it does not indicate immediate harm. Consult your doctor for personalized advice.
Check the batch number on the packaging. Affected batches are R56240011, R56240021, R56240031, R56240041, R56240051, R56240061, or R56240071.
The recall does not specify a remedy, so contact Westminster Pharmaceuticals for guidance.
We’ve drafted a message you can send Westminster Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0582-2025 — Westminster Pharmaceuticals Westminster Pharmaceuticals Hello, I own a Westminster Pharmaceuticals that is covered by recall D-0582-2025 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.
