Medline Industries recalled 175 arthroscopy kits on January 7, 2026. Calibration issues with sterilization equipment may impact product sterility. Patients and healthcare providers should stop using the devices immediately.
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.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Letter
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The recall involves Medline's arthroscopy kits, including models CDS984609B, DYNJ22501G, DYNJ32715F, DYNJ50834C, and DYNJ51069. The products were distributed worldwide and sold in the U.S. since their release.
Calibration issues with sterilization equipment may compromise the sterility assurance level (SAL) of the recalled products. This raises concerns about the potential for infections during surgical procedures.
There have been no reported injuries or incidents directly linked to the recalled products as of the recall date.
Stop using the recalled arthroscopy kits immediately. Contact Medline Industries or your healthcare provider for further instructions and to arrange for a refund.
For assistance, call Medline Industries at 1-800-396-9990 or visit their website for more information.
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