Medique recalls 2-count Pain-Off tablets with FDA CGMP deviations. Products not manufactured under current good practices. Check UPCs and expiration dates for affected lots.
CGMP Deviations: manufacturer recalled after an FDA inspection noted that these products were not manufactured under Current Good Manufacturing Practices.
Medique is recalling specific lots of Pain-Off pain relief tablets due to failure to meet FDA manufacturing standards. This means the products may not be safe or effective as intended.
The FDA found these products were not made according to current good manufacturing practices. This could mean the tablets might not be safe or effective, but the recall does not indicate immediate harm or injury.
People who purchased or use Medique Pain-Off tablets with the listed UPCs and expiration dates are affected. Those most at risk are individuals taking the medication for pain relief.
Check the UPC codes on the packaging: 3 47682 22847 7, 3 47682 22813 2, 3 47682 22833 0, or 3 47682 22864 4. Also look for expiration dates listed in the recall notice.
Verify your tablets match the UPC codes and expiration dates listed in the recall notice.
The FDA found these products were not manufactured under Current Good Manufacturing Practices.
Check the UPC codes on the packaging: 3 47682 22847 7, 3 47682 22813 2, 3 47682 22833 0, or 3 47682 22864 4. Also look for expiration dates listed in the recall notice.
The recall does not require stopping use immediately; check if your tablets match the affected lots before taking them.
We’ve drafted a message you can send Medique to request your refund or repair — edit it as you like.
Subject: Recall D-0390-2022 — Medique Medique Hello, I own a Medique that is covered by recall D-0390-2022 from Medique. 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.