RemedyRepack recalls Glimepiride 2mg tablets with specific NDC codes due to cGMP deviations. These tablets may not meet quality standards and should be checked for lot numbers.
cGMP Deviations
RemedyRepack is recalling Glimepiride 2 mg tablets in specific bottle counts and lot numbers because of manufacturing quality issues. This recall is important because the tablets may not meet the required quality standards, potentially affecting safety and effectiveness.
The recall is due to cGMP deviations, which means the manufacturing process did not meet quality standards. This could result in tablets that are not as effective or safe as they should be, but the risk is not described as causing serious injury.
People who have Glimepiride 2 mg tablets with the listed NDC codes and lot numbers are affected. Those taking this medication for diabetes management are most at risk.
Check if your Glimepiride 2 mg tablets are in 30-count or 90-count bottles with specific NDC codes (70518-0405-03 or 70518-0405-00) or 180-count bottles (70518-0405-02). Look for lot numbers and expiration dates listed in the recall notice.
Identify if your Glimepiride 2 mg tablets match the recalled NDC codes and lot numbers listed in the recall notice.
The recall is due to cGMP deviations, meaning the manufacturing process did not meet quality standards.
Check if your tablets match the recalled NDC codes and lot numbers. If they do, contact your doctor or pharmacist for advice.
The recall indicates potential quality issues, but the official notice does not specify a risk of serious injury or harm.
We’ve drafted a message you can send RemedyRepack to request your refund or repair — edit it as you like.
Subject: Recall D-0493-2023 — RemedyRepack RemedyRepack Hello, I own a RemedyRepack that is covered by recall D-0493-2023 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.
