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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Medline's arthroscopy kits are used in surgical procedures to assist with minimally invasive joint surgeries. They provide essential tools and materials necessary for arthroscopic surgeries.
The calibration issues with sterilization equipment may lead to insufficient sterilization of the products, increasing the risk of infection during surgical procedures.
This recall is not part of a broader industry pattern.
This recall affects healthcare providers and patients who may have used these kits, raising safety concerns about potential infections during surgeries.
Model numbers and lot numbers can typically be found on the product packaging or the device itself.
Expect a response for refund or replacement processing within 4-6 weeks.
Keep records of your purchase, including receipts, correspondence regarding the recall, and photos of the product.
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.
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