Medline recalls Proxima Drape surgical drapes due to potential pouch packaging breach that could compromise sterility. Affected items include specific model numbers and lot numbers.
Potential breach in pouch packaging which could lead to loss of sterility.
Medline is recalling certain Proxima Drape surgical drapes because the packaging might not stay sterile. This could lead to infections during surgery if the drapes are used without proper sterility.
The pouch packaging for these surgical drapes might not seal properly, which could allow contamination. If the drapes are not sterile when used, it could lead to infections during surgery.
Surgical teams and hospitals that use Medline Proxima Drape surgical drapes with the specific model numbers and lot numbers listed in the recall. Patients at risk during surgery if the drapes lose sterility.
Check for model numbers DYNJP1020S, DYNJP1025S, DYNJP1040, DYNJP1055S, DYNJP3000, DYNJP5050, DYNJP6060S, DYNJP9120A or lot numbers like 31124090044H. These drapes were sold with specific packaging labels.
Look for model numbers DYNJP1020S, DYNJP1025S, DYNJP1040, DYNJP1055S, DYNJP3000, DYNJP5050, DYNJP6060S, DYNJP9120A or lot numbers listed in the recall.
The pouch packaging might not seal properly, which could lead to loss of sterility during surgery.
Check the product labels for the model numbers or lot numbers listed in the recall. If you have the affected items, you should stop using them and contact Medline for further instructions.
Yes, model numbers DYNJP1020S, DYNJP1025S, DYNJP1040, DYNJP1055S, DYNJP3000, DYNJP5050, DYNJP6060S, DYNJP9120A and lot numbers like 31124090044H are affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1364-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1364-2025 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.
