BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD PYXIS¿ ES SERVER

    MDR report key: 25253837 · Received May 22, 2026

    Report

    Report Number
    2016493-2026-31245
    Event Type
    Malfunction
    Date Received
    May 22, 2026
    Date of Event
    April 27, 2026
    Report Date
    May 5, 2026
    Manufacturer
    CAREFUSION 303, INC.
    Product Code
    BRY
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    D4 AND H4 UNIQUE IDENTIFIER (UDI), MEDICAL DEVICE SERIAL, MEDICAL DEVICE MODEL, MEDICAL DEVICE CATALOG AND DEVICE MANUFACTURE DATE NOT AVAILABLE. UPON INVESTIGATION OF THE ACTUAL DEVICE USED IN THIS INCIDENT, IT WAS DETERMINED THAT THE MEDICATION WAS NOT CROSSING TO LOGISTICS FOR PYXIS. A TECHNICAL SUPPORT SPECIALIST (TSS) DIALED INTO CAREFUSION COORDINATION ENGINE, REVIEWED EXAMPLES AND CONFIRMED GHOST POCKET DISCREPANCIES, CLEARED AND REPOPULATED THE STATION INVENTORY IN THE CAREFUSION COORDINATION ENGINE DATABASE, INFORMED THE CUSTOMER, AND CONFIRMED THE ISSUE WAS RESOLVED WITH THE CUSTOMER REPORTING NORMAL OPERATION. 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, MEDICATION WAS NOT CROSSING TO LOGISTICS FOR PYXIS. MED ID "ERTA1VIA" (ERTAPENEM 1 GRAM VIAL) WAS NOT CROSSING TO LOGISTICS FOR STATION REPLENISHMENT. HOWEVER, THERE WERE NO DELAY TO PATIENT CARE AND ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS INCIDENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    348110 BD PYXIS¿ ES SERVER AUTOMATED DISPENSING CABINET BRY CAREFUSION 303, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1