Covidien recalls Polysorb Braided Absorb: 0-30" UNDYED HOS-11 (Lot A9J0018Y) due to potential packaging issues affecting sterility or humidity. Affected medical devices may cause infection if used improperly.
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 0 30" UNDYED HOS-11) because some packaging might not protect it from moisture or contamination. This could lead to infections if the suture is used in surgery without proper sterility.
The packaging may allow moisture or contaminants to enter, potentially compromising the suture's sterility. This could lead to infections if the suture is used in surgery without being properly sterilized.
Healthcare professionals and patients who received this specific suture product (Lot A9J0018Y) for soft tissue surgery or eye procedures. The risk is low for most users as the suture is used in controlled medical settings.
Check for the product name 'Polysorb Braided Absorbable Suture 0 30" UNDYED HOS-11' with item code CL537. The affected lot number is A9J0018Y, which expires August 31, 2024.
Look for the lot number A9J0018Y on the packaging or label of the suture product.
The recall is for specific packaging issues that could affect sterility. If you have the affected lot, contact the manufacturer for guidance on whether it's safe to use.
The recall does not specify a remedy, so check with the manufacturer or healthcare provider for advice on handling the product.
Look for the lot number A9J0018Y on the packaging of Polysorb Braided Absorbable Suture 0 30" UNDYED HOS-11 (item code CL537).
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-1275-2020 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-1275-2020 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.
