BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD PYXIS¿ ES SERVER

    MDR report key: 25253834 · Received May 22, 2026

    Report

    Report Number
    2016493-2026-31231
    Event Type
    Malfunction
    Date Received
    May 22, 2026
    Date of Event
    April 27, 2026
    Report Date
    April 30, 2026
    Manufacturer
    CAREFUSION 303, INC.
    Product Code
    BRY
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    D4 & H4: SERIAL NUMBER, UNIQUE DEVICE IDENTIFIER AND MANUFACTURER DATE NOT AVAILABLE. UPON INVESTIGATION OF THE ACTUAL DEVICE USED IN THIS INCIDENT, IT WAS DETERMINED THAT THE ORDERS WERE NOT CROSSING. A TECHNICAL SUPPORT SPECIALIST CONNECTED TO CAREFUSION COORDINATION ENGINE (CCE) AND FOUND THAT STR PROC 12019 WAS CORRUPT, WHICH CAUSED ORDER NUMBERS TO POPULATE TWICE. THIS PROCESS WAS REQUIRED FOR RDE ORDERS TO GENERATE ADMIT DISCHARGE TRANSFER (ADT) MESSAGES AND PREVENT DUPLICATE ORDER NUMBERS. ONCE RE-ESTABLISHED, ORDERS BEGAN APPEARING NORMALLY. THE SYSTEM FUNCTIONED AS INTENDED AFTER THE TECHNICAL SUPPORT SPECIALIST TROUBLESHOT THE DEVICE.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ ES SERVER ORDERS WERE NOT CROSSING FROM CERNER TO IVP. THE CUSTOMER STATED THAT THERE WAS A DELAY IN PATIENT CARE. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    347983 BD PYXIS¿ ES SERVER AUTOMATED DISPENSING CABINET BRY CAREFUSION 303, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1