Medline recalls Proxima Drape surgical drapes labeled MINOR PACK and LAPAROSCOPY due to potential pouch packaging breaches that could compromise sterility. Affected items have specific lot numbers and expiration dates.
Potential breach in pouch packaging which could lead to loss of sterility.
Medline is recalling Proxima Drape surgical drapes labeled as MINOR PACK and LAPAROSCOPY because their pouch packaging might not stay sealed, risking loss of sterility during surgery. This could lead to infections if the drapes are used improperly.
The pouch packaging might not stay sealed properly, which could allow contamination. If the drape loses sterility, it might cause infections during surgery if used without proper cleaning or sterilization.
Surgical teams and hospitals that use these specific Proxima Drape drapes for minor procedures and laparoscopy. The risk is highest for medical professionals handling the drapes in sterile environments.
Check for the product label indicating 'MINOR PACK' and 'LAPAROSCOPY'. Look for lot numbers like 25AMD464 (expires 11/30/2029) or 24JMC011 (expires 04/30/2029) on the packaging.
Look for the label indicating 'MINOR PACK' and 'LAPAROSCOPY' on the drape packaging.
Confirm the lot number matches the listed numbers (e.g., 25AMD464, 24JMC011) to identify affected items.
The recall is due to potential breaches in the pouch packaging that could lead to loss of sterility, increasing infection risk during surgery.
Check for the label 'MINOR PACK' and 'LAPAROSCOPY' and verify the lot numbers listed in the recall notice.
The recall does not specify a remedy, so contact Medline directly for guidance on handling affected items.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1366-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1366-2025 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.
