Cardinal Healthcare recalls 50mg Metoprolol Succinate Extended-Release Tablets due to potential temperature exposure during storage. This may affect product stability and safety.
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Cardinal Healthcare is recalling 50mg Metoprolol Succinate Extended-Release Tablets because they may have been exposed to temperatures outside the labeled storage conditions. This could affect product stability and safety.
The tablets may have been exposed to temperatures outside the labeled storage conditions during manufacturing or distribution. This could potentially affect the stability of the medication, though the recall does not specify serious injury risks.
Prescription holders of the 50mg Metoprolol Succinate Extended-Release Tablets with NDC 45963-676-96 and batch 2447J211. Patients taking this medication are most at risk if they have not been properly stored.
Check for the product name 'Metoprolol Succinate Extended-Release Tablets, USP, 50 mg, 1000 Tablets, Rx Only' with NDC code 45963-676-96 and batch number 2447J211. The product was manufactured by Teva Pharmaceuticals USA, Inc. in North Wales, PA.
Verify the NDC code 45963-676-96 and batch number 2447J211 on your medication label.
The recall states the product may have been exposed to temperatures outside labeled storage conditions, which could affect stability. However, the recall does not specify serious injury risks.
Check for the NDC code 45963-676-96 and batch number 2447J211 on your medication label.
The recall does not specify a remedy, so you should check with your healthcare provider or pharmacist for guidance.
We’ve drafted a message you can send Cardinal Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0191-2024 — Cardinal Healthcare Cardinal Healthcare Hello, I own a Cardinal Healthcare that is covered by recall D-0191-2024 from Cardinal Healthcare. 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.
