BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD PYXIS¿ ES SERVER

    MDR report key: 25160220 · Received May 13, 2026

    Report

    Report Number
    2016493-2026-28636
    Event Type
    Malfunction
    Date Received
    May 13, 2026
    Date of Event
    April 16, 2026
    Report Date
    April 21, 2026
    Manufacturer
    CAREFUSION 303, INC.
    Product Code
    BRY
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, 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 THE MULTIPLE DRUGS WERE DROPPING TO BE FILLED IN JUST-IN-TIME (JIT) WHEN THEY WERE NOT BELOW PAR OR WERE NOT CORRECTLY DROPPING. A TECHNICAL SUPPORT SPECIALIST LOGGED INTO THE SERVER AND RAN THE REQUIRED QUERY TO VERIFY THE TRIGGER REFERENCED IN THE KNOWLEDGE ARTICLE (KA) - "RESTOCK ORDER 5.2 - EXTRA REFILLS FOR MEDICATION SENT, CUR VALUE SAME FOR ALL DEVICES", CONFIRMED THAT THE TRIGGER FIX HAD ALREADY BEEN APPLIED. 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 MULTIPLE DRUGS WERE DROPPING TO BE FILLED IN JUST-IN-TIME (JIT) WHEN THEY WERE NOT BELOW PAR OR WERE NOT CORRECTLY DROPPING. 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
    611252 BD PYXIS¿ ES SERVER AUTOMATED DISPENSING CABINET BRY CAREFUSION 303, INC.

    Patients

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