RemedyRepack Inc. recalls 0.5mg Ropinirole tablets due to cGMP deviations in repackaging. Affected lots expire by July 2023. Consumers should check NDC and lot numbers.
cGMP Deviations
RemedyRepack Inc. is recalling 0.5 mg Ropinirole tablets in 90-count bottles because of manufacturing quality issues during repackaging. This recall affects people who have these specific lots and may pose a risk to safety.
The recall is due to cGMP deviations during repackaging, which means the manufacturing process did not meet quality standards. This could potentially lead to unsafe drug products, though the exact risk is not specified in the recall notice.
People with prescription Ropinirole 0.5 mg tablets in 90-count bottles repackaged by RemedyRepack Inc. are affected. Those with the specific lot numbers listed are most at risk.
Check for NDC 70518-2439-00 and lot numbers B1789178-080122 (expiring 07/31/2023) or B1675475-050522 (expiring 05/31/2023). The product is prescription-only and repackaged by RemedyRepack Inc.
Look for NDC 70518-2439-00 and lot numbers B1789178-080122 or B1675475-050522 on the packaging.
The recall is due to cGMP deviations during repackaging, which means the manufacturing process did not meet quality standards.
Check the product details to see if it matches the recalled lots. If it does, contact RemedyRepack Inc. for further instructions.
Look for NDC 70518-2439-00 and lot numbers B1789178-080122 (expiring 07/31/2023) or B1675475-050522 (expiring 05/31/2023).
We’ve drafted a message you can send RemedyRepack to request your refund or repair — edit it as you like.
Subject: Recall D-0494-2023 — RemedyRepack RemedyRepack Hello, I own a RemedyRepack that is covered by recall D-0494-2023 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.
