Ascend Laboratories recalls 50mg Metoprolol Succinate Extended-Release Tablets due to failed dissolution specification. This may affect medication effectiveness. Check NDC 67877-591-05 and lot numbers 21141321/21141322.
Failed Dissolution Specification
Ascend Laboratories is recalling Metoprolol Succinate Extended-Release Tablets (50mg) because they failed the dissolution test. This could mean the medication doesn't work properly when taken as intended.
The tablets failed the dissolution test, meaning they may not release the medication properly in the body. This could lead to the medication not working as intended, but it does not cause immediate harm or injury.
People who have the specific 500-tablet bottles with NDC 67877-591-05 and lot numbers 21141321 or 21141322. Those taking this medication for heart conditions are most at risk.
Check for the NDC code 67877-591-05 on the bottle. Look for lot numbers 21141321 or 21141322. The expiration date is January 31, 2023.
Look for the NDC code 67877-591-05 and lot numbers 21141321 or 21141322 on the bottle.
No immediate danger, but the tablets may not work properly due to failed dissolution testing.
Check for NDC 67877-591-05 and lot numbers 21141321 or 21141322 on the bottle.
Check your medication and contact your doctor or pharmacist for advice.
We’ve drafted a message you can send Ascend Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0171-2023 — Ascend Laboratories Ascend Laboratories Hello, I own a Ascend Laboratories that is covered by recall D-0171-2023 from Ascend Laboratories. 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.
