BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD PYXIS¿ ES SERVER

    MDR report key: 25228602 · Received May 20, 2026

    Report

    Report Number
    2016493-2026-30444
    Event Type
    Malfunction
    Date Received
    May 20, 2026
    Date of Event
    April 23, 2026
    Report Date
    May 9, 2026
    Manufacturer
    CAREFUSION 303, INC.
    Product Code
    BRY
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    LA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    D4 & H4: SERIAL NUMBER, UNIQUE DEVICE IDENTIFIER (UDI) AND MANUFACTURER DATE NOT AVAILABLE. UPON INVESTIGATION OF THE ACTUAL DEVICE USED IN THIS INCIDENT, IT WAS DETERMINED THAT NEW PATIENTS AND ORDERS WERE NOT CROSSING TO ALL PYXIS. A TECHNICAL SUPPORT SPECIALIST (TSS) CONFIRMED THAT THE ISSUE WAS RELATED TO CENTERPOINT. ONCE THE CENTERPOINT ISSUE WAS RESOLVED, PATIENT AND ORDER MESSAGES RESUMED CROSSING CORRECTLY TO ALL PYXIS DEVICES, RESTORING NORMAL FUNCTIONALITY. THE SYSTEM FUNCTIONED AS INTENDED AFTER THE TECHNICAL SUPPORT SPECIALIST INVESTIGATED THE ISSUE.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ ES SERVER, THE NEW PATIENTS AND NEW ORDERS WERE NOT CROSSING OVER. THERE WERE NO DELAY, NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    271977 BD PYXIS¿ ES SERVER AUTOMATED DISPENSING CABINET BRY CAREFUSION 303, INC. 500001002501

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown