BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PYXIS MEDSTATION ES SYSTEM

    MDR report key: 21543954 · Received March 7, 2025

    Report

    Report Number
    2016493-2025-06441
    Event Type
    Malfunction
    Date Received
    March 7, 2025
    Date of Event
    February 7, 2025
    Report Date
    March 7, 2025
    Manufacturer
    CAREFUSION 303
    Product Code
    BRY
    UDI-DI
    10885403512667
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    UPON INVESTIGATION OF THE ACTUAL DEVICE USED IN THIS INCIDENT, IT WAS DETERMINED THAT THE PATIENT ORDERS WERE NOT CROSSING TO PYXIS. THE TECHNICAL SUPPORT SPECIALIST CONFIRMED THAT THIS ISSUE MIGHT BE RESOLVED ON THE SAME DAY. THE SYSTEM FUNCTIONED AS INTENDED AFTER THE TECHNICAL SUPPORT SPECIALIST TROUBLESHOT THE DEVICE.

    Description of Event or Problem · 0

    IT WAS REPORTED WHEN USING THE BD PYXIS MEDSTATION SYSTEM THE PATIENT ORDERS WERE NOT CROSSING TO PYXIS. THE CUSTOMER REPORTED THAT PATIENTS ORDERS WERE NOT PROFILING, STOCK OUTS AND REFILLS WERE NOT CROSSING TO LOGISTICS. THE CUSTOMER STATED THAT THIS MALFUNCTION CAUSED A DELAY TO THE PATIENT CARE. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS INCIDENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    813539 PYXIS MEDSTATION ES SYSTEM AUTOMATED DISPENSING CABINET BRY CAREFUSION 303 323 10885403512667

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown