BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD PYXIS¿ ES SERVER

    MDR report key: 24911021 · Received April 17, 2026

    Report

    Report Number
    2016493-2026-22290
    Event Type
    Malfunction
    Date Received
    April 17, 2026
    Date of Event
    March 24, 2026
    Report Date
    March 31, 2026
    Manufacturer
    CAREFUSION 303, INC.
    Product Code
    BRY
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    D.4 & H.4: 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 LOADING AND PENDING MEDICATIONS WERE NOT CROSSING OVER TO LOGISTICS. A TECHNICAL SUPPORT SPECIALIST CHECKED THE INTERFACE AND FOUND A STORED PROCEDURE IN PLACE THAT BLOCKS DEVICES STARTING WITH 'ZZ' FROM RECEIVING MESSAGES. ONCE THE STATIONS WERE LIVE, THE IMPLEMENTATION TEAM WILL REMOVE THE 'ZZ' FROM THE DEVICE NAME, ALLOWING THE STATION TO BEGIN RECEIVING MESSAGES. CUSTOMER WAS INFORMED VIA EMAIL AND APPROVED CLOSURE OF THE CASE. THE SYSTEM FUNCTIONED AS INTENDED AFTER THE TECHNICAL SUPPORT SPECIALIST INVESTIGATED THE DEVICE.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ ES SERVER, THE CUSTOMER WAS LOADING AND PENDING MEDICATIONS INTO THE STATION, BUT THE TRANSACTIONS DID NOT CROSS OVER TO LOGISTICS FOR MEDICATION PULLING. HOWEVER, THERE WERE NO DELAYS OR ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    968233 BD PYXIS¿ ES SERVER AUTOMATED DISPENSING CABINET BRY CAREFUSION 303, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown SN: (B)(6), LOCATION: 8EAST.