Covidien recalls Polysorb 2/0 30" Violet GU-46 sutures due to potential packaging issues affecting humidity or sterility. Affected lots may not be sterile when used in surgery.
There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
Covidien is recalling specific lots of Polysorb braided absorbable sutures because the packaging might not keep them sterile or dry enough for surgery. This could lead to infections or other complications if used improperly.
The packaging may allow moisture or contaminants to enter, potentially compromising the sterility of the sutures. This could lead to infections or other complications during surgery if the sutures are not properly sterile.
Surgical professionals and hospitals using the specific lot numbers listed in the recall. Patients undergoing surgery with these sutures are at risk if the packaging fails.
Check for the lot number D7H0866X on the packaging. The product is a violet-colored suture with item code UL878, used for soft tissue surgery, expiring August 31, 2022.
Look for the lot number D7H0866X on the suture packaging.
The recall indicates potential packaging issues that could affect sterility, so it is not recommended for use until the recall is addressed.
Check the packaging for the lot number D7H0866X. If you have this lot, contact Covidien for instructions.
The recall is active until the affected items are addressed; there is no specific end date mentioned.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-1299-2020 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-1299-2020 from Covidien. 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.