Medline recalls sterile surgical drape Proxima Drape Face Lift due to potential pouch packaging breach that could compromise sterility. Affected units have specific lot numbers and serial codes.
Potential breach in pouch packaging which could lead to loss of sterility.
Medline is recalling sterile surgical drape products labeled 'Face Lift' because their pouch packaging might not stay sealed properly. This could lead to loss of sterility during medical procedures, which is dangerous for surgical patients.
The drape's pouch packaging might not stay sealed properly, which could allow contamination. If the drape loses sterility during surgery, it could lead to infections in patients.
Healthcare professionals using the drape for surgery or procedures are most at risk. Patients undergoing surgery with this drape could face infection risks if sterility is compromised.
Check for the lot number 24JMD608 (valid until 06/30/2026) on the packaging. The product has a unique identifier: case number 40195327695638 and individual unit number 10195327695637.
Look for the lot number 24JMD608 (valid until 06/30/2026) and unique identifiers on the packaging.
The recall states there's a potential risk of sterility loss, so it's not safe to use until the remedy is applied. However, the remedy is not specified in the record.
The recall record does not specify a remedy, so no action is required beyond checking the packaging details.
Check for lot number 24JMD608 (valid until 06/30/2026) and unique identifiers: case number 40195327695638 and individual unit number 10195327695637.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1367-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1367-2025 from Medline. 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.
