Teva recalls 25mg Metoprolol Succinate Extended-Release Tablets (100 and 1000 tablets) due to failed dissolution specifications. These tablets may not release medication properly, potentially affecting treatment effectiveness.
Failed Dissolution Specifications
Teva is recalling 25 mg Metoprolol Succinate Extended-Release Tablets in 100-tablet and 1,000-tablet bottles because they failed dissolution specifications. This means the medication might not release properly, which could affect how well your treatment works.
The tablets failed dissolution specifications, meaning they may not release medication at the intended rate. This could lead to inconsistent blood levels of the drug, potentially affecting treatment effectiveness without causing immediate harm.
People prescribed metoprolol succinate extended-release tablets by a doctor who own these specific bottle sizes (100 or 1000 tablets) are affected. Those with heart conditions requiring this medication are most at risk.
Check for bottles labeled 'Metoprolol Succinate Extended-Release Tablets, 25 mg' with 100 or 1000 tablets. The NDC numbers are 45963-709-11 for 100 tablets and 45963-709-96 for 1000 tablets.
Identify the NDC numbers: 45963-709-11 (100 tablets) or 45963-709-96 (1000 tablets).
The tablets failed dissolution specifications, meaning they may not release medication properly, which could affect treatment effectiveness.
No, the recall does not require stopping use. The remedy is not stated in the recall notice.
The recall notice does not specify a remedy, so contact your doctor or pharmacist for guidance.
We’ve drafted a message you can send Teva to request your refund or repair — edit it as you like.
Subject: Recall D-0354-2026 — Teva Teva Hello, I own a Teva that is covered by recall D-0354-2026 from Teva. 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.
