BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD PYXIS¿ MEDBANK MINI

    MDR report key: 24313621 · Received February 11, 2026

    Report

    Report Number
    2016493-2026-05795
    Event Type
    Malfunction
    Date Received
    February 11, 2026
    Date of Event
    December 11, 2024
    Report Date
    January 27, 2026
    Manufacturer
    CAREFUSION 303, INC.
    Product Code
    BRY
    UDI-DI
    10885403512582
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    A REVIEW OF THE COMPLAINT HISTORY FOR SN (B)(6) WAS PERFORMED IN SALESFORCE WHICH DID NOT LOCATE SIMILAR COMPLAINTS WITH THE SAME FAILURE MODE FOR THIS SERIAL NUMBER. A REVIEW OF THE DEVICE HISTORY RECORD FOR SN (B)(6) WAS PERFORMED FROM THE DATE OF MANUFACTURE, 22-APR-2021 AND CONFIRMED THAT THIS DEVICE WAS NOT PREVIOUSLY RETURNED FOR SERVICING AND THERE WERE NO PRODUCTION FAILURES WHICH CORRELATES TO THE CUSTOMER REPORTED ISSUE. UPON INVESTIGATION OF THE ACTUAL DEVICE USED IN THIS INCIDENT, IT WAS DETERMINED THAT THE DEVICE HAD RESTOCKING ISSUE IN 05 17 THAT ARE CAUSING THE CUBIES TO NOT BE RECOGNIZED AND EJECTING THEM OUT. A FIELD SERVICE ENGINEER WORKED WITH MEDBANK/CUBEX AND DETERMINED THAT THE ISSUE WAS CAUSED BY A DEFECTIVE ROW TRAY. THEY REPLACED THE FAULTY ROW TRAY AND VERIFIED THAT ALL QBS IN THE DRAWER WERE OPERATING CORRECTLY. WHILE ON SITE, THE TECHNICIAN WAS ALSO ASKED TO REVIEW SEVERAL ADDITIONAL COMPONENTS AND CASES, AND TOGETHER THEY RESOLVED ALL REMAINING ISSUES ASSOCIATED WITH THE MEDBANK TOWER. THE SYSTEM FUNCTIONED AS INTENDED AFTER THE FIELD SERVICE ENGINEER REPAIRED THE DEVICE.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDBANK MINI HAD RESTOCKING ISSUES IN 05 17 WHICH CAUSED THE CUBIES TO NOT BE RECOGNIZED AND EJECT THEM OUT. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    374067 BD PYXIS¿ MEDBANK MINI AUTOMATED DISPENSING CABINET BRY CAREFUSION 303, INC. 500004500500 10885403512582

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown