Teva recalls 50mg Metoprolol Succinate Extended-Release Tablets (100 and 1,000 tablets) due to failed dissolution specifications. These tablets may not release medication properly, potentially affecting treatment effectiveness.
Failed Dissolution Specifications
Teva is recalling 50 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 correct rate. This could lead to inconsistent blood levels of the drug, potentially affecting how well the medication works for heart conditions.
People who have the specific 50 mg Metoprolol Succinate Extended-Release Tablets bottles with the listed lot numbers and expiration dates are affected. Those taking this medication for heart conditions are most at risk.
Check for 50 mg Metoprolol Succinate Extended-Release Tablets bottles with NDC numbers 45963-676-11 (100 tablets) or 45963-676-96 (1,000 tablets). Look for lot numbers 0486G251, 0487G251, 0488G251 or 0486G252, 0487G253, 0488G252 with expiration dates of January 2027.
Verify the NDC numbers and lot numbers listed in the recall notice to confirm if your tablets are affected.
The recall is due to failed dissolution specifications, which may affect how well the medication works. Do not use these specific bottles until you confirm they are not recalled.
Check the NDC numbers and lot numbers to see if your tablets are affected. If they are, contact your doctor or pharmacist for guidance.
Look for NDC numbers 45963-676-11 (100 tablets) or 45963-676-96 (1,000 tablets) with lot numbers 0486G251, 0487G251, 0488G251 or 0486G252, 0487G253, 0488G252 and expiration date January 2027.
We’ve drafted a message you can send Teva to request your refund or repair — edit it as you like.
Subject: Recall D-0355-2026 — Teva Teva Hello, I own a Teva that is covered by recall D-0355-2026 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.
