Andover Healthcare recalls Sterile Co-Flex Med 3" single-use wound dressings due to incomplete packaging seals that could compromise sterility during use.
Incomplete packaging seal of sterile product
Andover Healthcare is recalling Sterile Co-Flex Med 3" single-use wound dressings because their packaging seals may be incomplete. This could allow contamination of the sterile product, increasing infection risk during medical use.
Incomplete packaging seals could allow contaminants to enter the sterile product during use. This might lead to infection if the dressing is not properly sterile when applied to wounds or injuries.
Healthcare professionals and patients using the Sterile Co-Flex Med 3" wound dressings for secondary wound care or compression wraps. Those with the specific lot number CI10LN are most at risk.
Check for the product name 'Sterile Co-Flex Med 3"' and lot number CI10LN on the packaging. The expiration date range is from October 1, 2021 to June 14, 2022.
Look for the lot number CI10LN on the packaging of the Sterile Co-Flex Med 3" wound dressing.
The recall is due to incomplete packaging seals that could compromise sterility. If you have the lot number CI10LN, you should check with the manufacturer before use.
The recall does not specify a remedy, so you should check the packaging for the lot number CI10LN and contact Andover Healthcare for further instructions.
Look for the product name 'Sterile Co-Flex Med 3"' and lot number CI10LN on the packaging. The expiration date range is from October 1, 2021 to June 14, 2022.
We’ve drafted a message you can send Andover Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0183-2020 — Andover Healthcare Andover Healthcare Hello, I own a Andover Healthcare that is covered by recall Z-0183-2020 from Andover Healthcare. 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.
