Medline recalls specific arthroscopy kits due to potential sterility risks from calibration errors in sterilization packaging. Affected products include CDS984609B and DYNJ22501G models with certain lot numbers.
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 arthroscopy convenience kits that may not be sterile due to calibration issues in the sterilization process. This could lead to infections if the kits are used in medical procedures.
The calibration issues in the sterilization equipment might compromise the sterility assurance level of the kits. This means the kits could become contaminated during the packaging process, increasing infection risk during surgery.
Healthcare professionals using the recalled arthroscopy kits for surgical procedures are most at risk. Patients receiving these kits during surgery could potentially be exposed to infection.
Check for model numbers CDS984609B or DYNJ22501G with specific lot numbers listed in the recall notice. The kits are sold under Medline's convenience kit line for arthroscopy procedures.
Identify the model number on the kit (CDS984609B or DYNJ22501G) and compare with the listed lot numbers in the recall notice.
Reach out to Medline directly for assistance with the recall process if you have the affected product.
Medline identified calibration issues in the sterilization equipment that could impact the sterility assurance level of the kits.
The recall indicates potential sterility risks, so affected kits should not be used until the issue is resolved.
Check the model number and lot number against the list 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-2127-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2127-2026 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.
