RemedyRepack recalls Carvedilol 25mg tablets due to unsafe N-Nitroso Carvedilol Impurity-1 levels. Affected lots expire May 2025 and July 2025. Stop using immediately if you have these specific lots.
CGMP deviations: presence of N-Nitroso Carvedilol Impurity-1 (NNC 1), above the FDA recommended acceptable intake limit.
RemedyRepack is recalling Carvedilol 25 mg tablets that contain an unsafe chemical impurity. This impurity could pose a health risk if taken in amounts exceeding the FDA's safety limits.
The tablets contain N-Nitroso Carvedilol Impurity-1 (NNC 1) at levels above the FDA's acceptable limit. This impurity could potentially cause health issues if consumed in the amounts that exceed the safe threshold.
People with prescriptions for Carvedilol 25 mg tablets from the specific lots listed (J0777493050824 and J0787856062124) are affected. Those who have taken these tablets without medical supervision are at risk.
Check the blister pack for the lot numbers J0777493050824 or J0787856062124. These tablets were manufactured by Glenmark in Mahwah, NJ and repackaged by RemedyRepack in Indiana, PA.
If you have the recalled lot numbers, stop using these tablets right away.
The FDA found that the Carvedilol tablets contain N-Nitroso Carvedilol Impurity-1 at levels above the acceptable limit.
Stop using them immediately and contact your doctor for guidance.
No, only the specific lot numbers listed in the recall.
We’ve drafted a message you can send RemedyRepack to request your refund or repair — edit it as you like.
Subject: Recall D-0217-2025 — RemedyRepack RemedyRepack Hello, I own a RemedyRepack that is covered by recall D-0217-2025 from RemedyRepack. 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.