Medline recalls 351 surgical drapes due to potential sterility issues from calibration problems in sterilization equipment. All products were exposed to validated cycles but calibration issues may impact sterility assurance levels.
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
Medline is recalling 351 surgical drapes because calibration problems in the sterilization equipment used to package them could reduce the sterility assurance level. This means the drapes might not be sterile as claimed, which is risky for medical procedures.
The sterilization equipment used to package the drapes had calibration issues that could affect the sterility assurance level (SAL). This means the drapes might not be sterile as intended, increasing infection risk during medical procedures.
Healthcare professionals and medical facilities that use these surgical drapes for procedures. The risk is primarily for infections during surgeries if the drapes are not properly sterile.
Check for the model numbers listed in the recall: DYNJP2410 through DYNJP2498. These drapes are sold in various sizes and types, including sterile and economy options, with specific lot numbers and UDI-DI codes.
Look for the model numbers (DYNJP2410 to DYNJP2498) and lot numbers on the drapes or packaging to confirm if they are recalled.
The recall indicates potential sterility issues, so they should not be used until confirmed safe. The manufacturer has identified calibration problems that could impact sterility assurance levels.
Check the model numbers (DYNJP2410 to DYNJP2498) and lot numbers on the drapes or packaging. The recall includes specific product details and lot numbers listed in the official notice.
The recall does not specify a return process or remedy, so the manufacturer has not provided instructions for disposal or replacement.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2128-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2128-2026 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.
