Medline recalls specific Proxima Drape surgical products due to potential pouch packaging breaches that could compromise sterility during medical procedures.
Potential breach in pouch packaging which could lead to loss of sterility.
Medline is recalling certain Proxima Drape surgical drapes because their packaging might not stay sterile. This could lead to infections if used in surgery without proper sterility.
The pouch packaging may breach, leading to loss of sterility. This could cause infections if the drapes are used in surgical procedures without being sterile.
Surgical staff and hospitals that use the recalled Proxima Drape products. Patients at risk during surgery if the drapes are used without sterility.
Check for product labels with specific model numbers like DYNJCDCSEC01 or lot numbers such as 45024100168. The drapes are used in surgical settings and come with unique UDI codes.
Look for model numbers such as DYNJCDCSEC01 or lot numbers like 45024100168 on the drapes.
The recall is due to potential breaches in the pouch packaging that could lead to loss of sterility during surgical procedures.
Check the product labels for model numbers or lot numbers listed in the recall notice and contact Medline for further instructions.
Yes, if the packaging breaches and the drapes are not sterile, this could lead to infections during surgery.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1363-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1363-2025 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.
