Covidien recalls Kerlix Gauze Rolls with potential sterility breach due to seal defects. Affected lots 18E030462, 18E223262, 18F122962. Stop using if you have these items.
Potential for product sterility breach due to a compromised or pinched seal defect
Covidien is recalling Kerlix gauze rolls that may have a seal defect causing sterility breaches. This could lead to infections if used for wounds. The recall affects specific lot numbers.
The gauze rolls may have a pinched or compromised seal that allows bacteria to enter. This could breach sterility and cause infections if the product is used on wounds.
People who own or use Kerlix gauze rolls with lot numbers 18E030462, 18E223262, or 18F122962 are affected. Those using the product for wound dressing are most at risk.
Check the lot number on the packaging. Affected lots are 18E030462, 18E223262, and 18F122962. The product is a 6-ply gauze roll used for bandaging wounds.
Look for lot numbers 18E030462, 18E223262, or 18F122962 on the packaging.
The recall is due to a potential seal defect that could cause sterility breaches, increasing infection risk during wound dressing.
Check the lot number on your packaging. If it matches the affected lots, stop using the gauze roll and contact Covidien for instructions.
The recall record does not mention a fix or remedy. Affected products should be stopped use and disposed of.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-0015-2019 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-0015-2019 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.
