Covidien recalls specific Polysorb Braided Absorbable Suture 3/0 3:0 VIOLET GS-11 (Lot A9H1170Y) due to potential packaging issues affecting humidity or sterility. Affected medical devices may not be sterile when used.
There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
Covidien is recalling a specific type of surgical suture (Polysorb Braided Absorbable Suture 3/0 30 VIOLET GS-11) because some packaging might not keep it sterile or dry. This could lead to infections or other complications during surgery if the suture is used without proper sterility.
The packaging might not properly protect the suture from moisture or contaminants. If the suture becomes wet or contaminated, it could lose its sterility and cause infections during surgery.
Healthcare professionals using this suture for soft tissue or eye surgeries may be affected. Patients undergoing procedures with this suture could be at risk if the packaging fails.
Check for the item code CL815 and lot number A9H1170Y on the packaging. This suture is used for soft tissue or eye surgeries and expires July 31, 2024.
Look for the item code CL815 and lot number A9H1170Y on the 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 item code CL815 and lot number A9H1170Y. If you have it, contact the manufacturer for guidance.
No, this suture is indicated for soft tissue approximation or eye surgeries, not cardiovascular or neural tissue.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-1277-2020 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-1277-2020 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.
