Covidien recalls Dermacea Gauze Fluff Rolls with potential sterility breach due to seal defects. Affected lots include 18D180762 through 18F122462. 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 Dermacea Gauze Fluff Rolls that may have a seal defect causing sterility breaches. This could lead to infections if used for wound dressing. Affected products include specific lot numbers listed in the recall.
The gauze rolls may have a compromised seal that allows bacteria to enter, potentially causing infections. This risk is higher when used on open wounds or cuts where sterility is critical.
People who own or use Dermacea Gauze Fluff Rolls for wound dressing, especially those with open wounds or recent injuries. Those using the product for medical purposes are most at risk.
Check the product label for lot numbers starting with 18D180762 through 18F122462. The product is a 6-ply gauze roll measuring 4 x 4-1/8 yards (10.2 cm x 3.7 m).
Look for lot numbers on the product label that match the affected ranges: 18D180762 through 18F122462.
The gauze rolls may have a seal defect that could lead to sterility breaches, increasing infection risk during wound dressing.
Check the product label for lot numbers starting with 18D180762 through 18F122462. The product is a 6-ply gauze roll measuring 4 x 4-1/8 yards (10.2 cm x 3.7 m).
The recall does not specify a remedy, so contact Covidien directly for instructions on how to handle the product.
We’ve drafted a message you can send Covidien to request your refund or repair — edit it as you like.
Subject: Recall Z-0018-2019 — Covidien Covidien Hello, I own a Covidien that is covered by recall Z-0018-2019 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.
