Glenmark Pharmaceuticals recalls 12.5mg Carvedilol tablets due to manufacturing deviations. Affected lots expire Jan 2026. Consumers should contact the company for details.
CGMP Deviations
Glenmark Pharmaceuticals is recalling 12.5mg Carvedilol tablets that were manufactured with CGMP deviations. This means the product may not be safe for use as intended, though the exact risk isn't specified in the recall notice.
CGMP deviations refer to manufacturing process failures that could affect product safety. These deviations might mean the tablets don't meet quality standards, but the recall doesn't specify how this could cause harm.
People with prescriptions for Carvedilol tablets who received these specific lots from Glenmark Pharmaceuticals Inc. in the US. Those with heart conditions or high blood pressure are most at risk.
Check for the product name 'Carvedilol Tablets, USP 12.5 mg, 500-count bottle, Rx Only'. Look for lot numbers 17240238, 17240243, or 17240245 with expiration dates of January 2026.
Reach out to Glenmark Pharmaceuticals Inc. for specific instructions on what to do with the recalled product.
The recall is due to CGMP deviations, which are manufacturing process failures that could affect product safety.
Contact Glenmark Pharmaceuticals Inc. for specific instructions on what to do with the recalled product.
The recall does not specify the exact safety risks, but the CGMP deviations could mean the product is not safe as intended.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0336-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0336-2025 from Glenmark. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
