Covidien recalls 100% cotton Kerlix bandage rolls with potential sterility breach due to seal defects. Affected lots include 18D181262 through 18F158362. Consumers should check product details and contact for remedy.
Potential for product sterility breach due to a compromised or pinched seal defect
Covidien is recalling certain Kerlix bandage rolls that may have a seal defect causing sterility breaches. This could lead to infections if the bandage is used improperly. Affected products include specific lot numbers listed in the recall notice.
The bandage roll may have a pinched or compromised seal, which could allow bacteria to enter the wound during use. This risk is related to the product's sterility and not a physical hazard like fire or injury.
Users of Kerlix bandage rolls with the listed lot numbers are affected. People applying bandages to wounds or injuries are most at risk if the seal defect compromises sterility.
Check the product label for lot numbers starting with 18D181262 through 18F158362. The bandage roll is 100% cotton, 6 layers, large size (4-1/2 x 4-1/8 yd).
Look for lot numbers starting with 18D181262 through 18F158362 on the bandage roll.
The recall is due to potential sterility breaches from a seal defect that could allow bacteria to enter wounds.
Check the product label for lot numbers starting with 18D181262 through 18F158362.
The recall does not specify a remedy, so contact Covidien directly for further instructions.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-0014-2019 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-0014-2019 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.
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.
