Medline Industries recalled 1,070 ADMIT KITS due to calibration issues affecting sterilization. The recall, effective January 7, 2026, has been classified as Class II. Healthcare providers must stop using these kits immediately to ensure patient safety.
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 Medline ADMIT KIT is used in healthcare settings for patient admission procedures. These kits typically include various sterile medical devices necessary for initial patient care.
The calibration issues in the sterilization equipment may lead to inadequate sterilization of the kits, increasing the risk of infection for patients.
This recall is not part of a broader industry pattern.
Consumers and healthcare providers face potential health risks from using non-sterile kits. Immediate action is necessary to prevent possible infections.
Model and lot numbers are typically printed on the packaging or on the kit itself.
Expect a timeframe of 4-6 weeks for refund processing after following the recall instructions.
Document your communications regarding the recall, including dates and details of your interactions.
The recalled ADMIT KITS have model number DYKA1343A and include several lot numbers: 25LBC732, 25FBN781, 25DBK346, 24IBD021, and 24DBK171. The products were distributed worldwide, including across the United States, and were sold in multiple healthcare settings.
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