Medline recalls specific arthroscopy kits due to potential sterility assurance level issues from calibration problems in sterilization packaging cycles.
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 because of 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 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 be exposed to infection.
Check for model numbers CDS984609B or DYNJ22501G on the kits. Look for lot numbers starting with 21, 22, or 23 in the product description.
Review the model number and lot number on the kit to confirm if it's in the recalled list.
Medline identified calibration issues in the sterilization equipment that could impact the sterility assurance level of the kits.
The recalled models include ARTHROSCOPY CDS (CDS984609B) and ARTHROSCOPY TRAYS (DYNJ22501G).
Check for model numbers CDS984609B or DYNJ22501G and lot numbers starting with 21, 22, or 23.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1422-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1422-2026 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.
