Ascend Laboratories recalls 25mg Metoprolol Succinate Extended-Release Tablets due to failed dissolution specifications. This may affect medication effectiveness. Check NDC 67877-590-01 and lot #21143093 for affected products.
Failed Dissolution Specifications.
Ascend Laboratories is recalling Metoprolol Succinate Extended-Release Tablets (25mg) because they failed dissolution specifications. This could mean the medication doesn't work as intended, which is serious for people taking it for heart conditions.
The tablets failed to dissolve properly as they should, which could lead to inconsistent medication levels in the body. This might not cause immediate harm but could affect how well the medication works over time for heart conditions.
People with prescriptions for Metoprolol Succinate Extended-Release Tablets (25mg) who bought the product between January 2023 and March 2023. Those with heart conditions are most at risk.
Check for the NDC code 67877-590-01 and lot number 21143093 on the product label. The product was manufactured in India and distributed by Ascend Laboratories in the U.S. between January 2023 and March 2023.
Look for NDC 67877-590-01 and lot number 21143093 on the bottle.
The recall is due to failed dissolution specifications, which could affect medication effectiveness. The product may not work as intended, but the remedy is not stated in the record.
Check for NDC 67877-590-01 and lot number 21143093 on the product label. The product was manufactured in India and distributed by Ascend Laboratories in the U.S. between January 2023 and March 2023.
The recall record does not specify a remedy, so the official notice does not say what to do next.
We’ve drafted a message you can send Ascend Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0393-2022 — Ascend Laboratories Ascend Laboratories Hello, I own a Ascend Laboratories that is covered by recall D-0393-2022 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.
