Andover Healthcare recalls Sterile Co-Flex LF2 3" single-use wound dressings due to incomplete packaging seal risking contamination. Affected items have specific lot numbers and expiration dates.
Incomplete packaging seal of sterile product
Andover Healthcare is recalling Sterile Co-Flex LF: 3" single-use wound dressings because their packaging seal may be incomplete. This could lead to contamination of the sterile product, making it unsafe for medical use.
The packaging seal may not be complete, which could allow contamination of the sterile product. This means the dressing might not be sterile when applied to a wound or injury, increasing infection risk.
Healthcare professionals and patients using the Sterile Co-Flex LF2 3" wound dressings for secondary wound care or compression wraps. Those with the specific lot numbers and expiration dates listed are most at risk.
Check for the product name 'Sterile Co-Flex LF2 3"' and the lot numbers: CIOZJV, CI02SW, CI18YA, CI1FJ2. The expiration date ranges from October 1, 2021, to June 14, 2022.
Look for the lot numbers CIOZJV, CI02SW, CI18YA, or CI1FJ2 on the packaging.
The recall is due to a potential packaging seal issue that could lead to contamination. If the seal is incomplete, the product may not be sterile and should not be used.
Check the lot numbers on the packaging. If it matches the listed numbers, contact Andover Healthcare for guidance.
The affected products have specific lot numbers: CIOZJV, CI02SW, CI18YA, CI1FJ2, and expire between October 1, 2021, and 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-0181-2020 — Andover Healthcare Andover Healthcare Hello, I own a Andover Healthcare that is covered by recall Z-0181-2020 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.
