Medline Industries recalled 32 units of Convenience Kits on January 7, 2026. Issues with sterilization equipment calibration may compromise device safety. Users should stop using the products immediately and follow recall instructions.
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 Convenience Kits are utilized in healthcare settings to provide essential medical supplies in a sterile environment. Consumers and healthcare providers purchase these kits for various medical procedures.
Calibration issues with the sterilization equipment may lead to a lack of proper sterilization of medical devices, posing a risk of infection to patients.
This recall is not part of a broader industry pattern.
The recall poses a significant health risk, requiring immediate action from users. Patients and healthcare providers must discontinue use and follow the manufacturer's instructions to avoid potential complications.
The model number and lot number can typically be found on the packaging or on a label attached to the product itself.
Expect a refund or replacement process to take approximately 4-6 weeks once the return is initiated.
Keep copies of all correspondence, receipts, and any documentation related to the product and recall.
The recalled product includes the Medline Convenience Kits, Model Number DYNJ50806L. These kits were distributed worldwide, including the US, and the recall affects 32 units.
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