Medline Industries recalled 14.9 million surgical drapes on January 7, 2026. Calibration issues with sterilization equipment may impact sterility assurance levels. Patients and healthcare providers must stop using these products 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 surgical drapes are used in medical settings to maintain a sterile environment during procedures. They are essential for preventing infections and ensuring patient safety.
The calibration issues with sterilization equipment may result in non-sterile drapes reaching patients, increasing the risk of infections during surgeries.
This recall is not part of a broader industry pattern.
Healthcare providers must urgently stop using the affected drapes, which disrupts operations and compromises patient safety.
Model numbers can be found on the product packaging or labels attached to the surgical drapes.
Expect 4-6 weeks for refund processing after the returned products are received.
Keep copies of receipts, any correspondence with Medline, and photos of the product for your records.
The recall affects various models of Medline surgical drapes, including DYNJP2410 and DYNJP2411. These products were distributed worldwide, with a total of 14,927,765 units recalled.
Not sure what to do next? Our guide walks you through the process step by step.
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