Covidien recalls Polysorb Braided Absorbable Suture 2-0 VIOLET 30" V-20 (Lot A9J0421Y) due to potential packaging issues affecting humidity or sterility. Affected medical devices may not be safe for surgery.
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 2-0 VIOLET 30" V-20) because some packaging might not keep it sterile or dry enough. This could lead to infections or other problems during surgery if the suture is used improperly.
The packaging might not properly protect the suture from moisture or contamination, which could compromise its sterility. If the suture is not sterile when used, it could cause infections or other complications during surgery.
Healthcare professionals using this suture for soft tissue surgery or eye procedures may be affected. Patients undergoing surgery with this specific suture could be at risk if the packaging integrity is compromised.
Check for the item code GL123 on the packaging. The specific lot number A9J0421Y and expiration date of August 31, 2024 are also listed on the product.
Look for the item code GL123 and lot number A9J0421Y on the suture packaging.
The recall indicates potential packaging issues that could affect sterility or humidity, so it is not recommended for use until the recall is addressed.
The recall does not specify a remedy, so check the packaging for the item code and lot number to determine if it is affected.
Look for the item code GL123 and lot number A9J0421Y on the packaging. The expiration date is August 31, 2024.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-1286-2020 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-1286-2020 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.
