Covidien recalls specific Polysorb suture lots due to potential packaging issues that could affect humidity or sterility. Affected items may not be safe for medical use.
There is a potential for packaging integrity issues impacting the humidity or sterility barrier of specific production lots.
Covidien is recalling certain Polys: 2-0 UNDYED 30" V-20 sutures with item code GL323. The recall is because specific production lots might have packaging that doesn't protect against humidity or contamination, which could make the suture unsafe for medical procedures.
The packaging might not properly block humidity or contaminants, which could compromise the suture's sterility. This could lead to infections or other complications during medical procedures if the suture is used without proper sterility.
Healthcare professionals using the specific suture lot (A9J0384Y) for soft tissue or eye surgery. Patients receiving this suture during procedures are at risk if the packaging fails.
Check for the item code GL323 on the packaging. The specific lot number A9J0384Y with expiration date August 31, 2024 is affected. This suture is used for soft tissue or eye surgery, not heart or nerve procedures.
Look for the item code GL323 and lot number A9J0384Y on the packaging.
No, this specific lot is recalled due to potential packaging issues that could affect sterility. It is intended for soft tissue or eye surgery only.
Check for item code GL323 and lot number A9J0384Y with expiration date August 31, 2024.
The recall does not specify a remedy, so contact the manufacturer for guidance.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-1289-2020 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-1289-2020 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.
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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.
