Glenmark Pharmaceuticals recalls 40mg Rosuvastatin tablets due to CGMP deviations. This affects specific batch numbers and expiration dates. Consumers should check their product details and contact the manufacturer for guidance.
CGMP Deviations
Glenmark Pharmaceuticals is recalling 40mg Rosuvastatin tablets that were manufactured with CGMP deviations. This means the medication may not meet quality standards, though the recall does not specify immediate health risks.
CGMP deviations refer to issues in the manufacturing process that could affect the quality of the medication. This means the tablets might not be as safe or effective as they should be, but the recall does not indicate a risk of serious injury.
People who have the specific batch numbers listed in the recall notice. Those with a prescription for this medication are most at risk.
Check the product label for the batch number and expiration date. The affected tablets have specific batch numbers and expiration dates listed in the recall notice.
Look for the batch number and expiration date on the tablet packaging to determine if it is affected.
The recall does not specify that the medication is unsafe; it indicates potential quality issues due to CGMP deviations.
Check the batch number and expiration date on the packaging against the specific numbers listed in the recall notice.
The recall does not require stopping use; it only indicates potential quality issues that may need attention.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0339-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0339-2025 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.
