Medline recalls surgical packs with potential sterility issues due to calibration problems in sterilization equipment. Affected products include specific models and lot numbers listed in the recall notice.
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 surgical packs that may not be sterile due to calibration issues in the sterilization equipment used to package them. This could lead to infections if the packs are used in medical procedures.
The sterilization equipment used to package these surgical packs had calibration issues, which could affect the sterility assurance level (SAL). This means the packs might not be sterile when used in medical procedures, potentially leading to infections.
Healthcare professionals and medical facilities that use Medline surgical packs. The risk is primarily for those using the packs in surgical procedures where sterility is critical.
Check for the model number DYNJP1050UG or DYNJP8401 with specific lot numbers listed in the recall notice. The affected packs have UDI-DI codes starting with 10080196573509 or 10080196740710.
Look for the model number DYNJP1050UG or DYNJP8401 and the specific lot numbers listed in the recall notice.
Medline identified calibration issues in the sterilization equipment used to package these surgical packs, which could impact the sterility assurance level.
The recall does not specify a remedy, so no immediate action is required beyond checking if your product is affected.
Check the model number and lot number against the list of affected products provided in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2130-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2130-2026 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.
