Covidien recalls Polysorb Braided Absorb: 3/0 30" UNDYED V-20 (Lot D7G0387X) due to potential packaging issues affecting humidity or sterility. Affected medical devices may not be sterile.
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" UNDYED V-20) 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 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 product name 'Polysorb Braided Absorbable Suture 3/0 30" UNDYED V-20' with item code GLS322. The affected lot number is D7G0387X, expiring July 31, 2022.
Inspect the packaging for signs of moisture or damage that might indicate compromised sterility.
The recall indicates potential packaging issues that could affect sterility, so it is not recommended for use until the issue is resolved.
The recall does not specify a remedy, so contact the manufacturer for guidance on safe handling or disposal.
Check for the lot number D7G0387X on the packaging, which expires July 31, 2022.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-1290-2020 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-1290-2020 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.
