Ascend Laboratories recalls 25mg metoprolol succinate extended-release tablets due to failed dissolution specifications. This may affect medication effectiveness. Contact for remedy details.
Failed Dissolution Specifications
Ascend Laboratories is recalling 25mg metoprol:ol succinate extended-release tablets that may not dissolve properly. This could lead to incorrect medication dosing if taken as intended.
The tablets may not dissolve correctly in the stomach, leading to inconsistent medication release. This could cause incorrect dosing levels if taken as intended.
People prescribed metoprolol succinate 25mg tablets by a doctor. Those with heart conditions or high blood pressure are most at risk.
Check for the product name 'Metoprolol Succinate Extended-Release Tablets, USP, 25 mg* Rx Only'. Look for lot number 25140859 and expiration date January 2027 on the packaging.
Look for lot number 25140859 and expiration date January 2027 on the packaging.
The recall is due to failed dissolution specifications, which may affect medication effectiveness. Consult your doctor before taking.
Check for lot number 25140859 and expiration date January 2027 on the packaging.
The recall does not specify a remedy, so contact your doctor or the manufacturer for guidance.
We’ve drafted a message you can send Ascend Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0547-2026 — Ascend Laboratories Ascend Laboratories Hello, I own a Ascend Laboratories that is covered by recall D-0547-2026 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.
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