Rubicon Research recalls 25mg Metoprolol Tartrate tablets due to metal contamination. This could cause injury if swallowed. Contact TruPharma for details.
Presence of Foreign Substance: metal in tablet
Rubicon Research is recalling 25mg Metoprolol Tartrate tablets that may contain metal. This could cause injury if taken. The recall is for prescription-only medication distributed by TruPharma.
Metal particles in the tablets could cause injury if swallowed. This is a foreign substance that might lead to harm in the digestive tract.
Prescription holders of Metoprolol Tartrate tablets from this specific batch. People taking this medication are most at risk.
Check for the 25mg Metoprolol Tartrate tablets with NDC 52817-360-00, lot number 231037H1, and expiration date 6/2027. The product is prescription-only and distributed by TruPharma.
Look for the NDC code 52817-360-00 and lot number 231037H1 on the bottle.
The recall states metal may be present, which could cause injury if swallowed. Do not take these tablets.
Check for NDC 52817-360-00, lot 231037H1, and expiration 6/2027 on the bottle.
The recall does not specify a remedy. Contact TruPharma for guidance.
We’ve drafted a message you can send Rubicon Research to request your refund or repair — edit it as you like.
Subject: Recall D-0517-2024 — Rubicon Research Rubicon Research Hello, I own a Rubicon Research that is covered by recall D-0517-2024 from Rubicon Research. 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.
