BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD PYXIS¿ MEDBANK TOWER AUX

    MDR report key: 24543693 · Received March 9, 2026

    Report

    Report Number
    2016493-2026-12049
    Event Type
    Malfunction
    Date Received
    March 9, 2026
    Date of Event
    February 11, 2026
    Report Date
    February 16, 2026
    Manufacturer
    CAREFUSION 303, INC.
    Product Code
    BRY
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, 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 OF THIS INCIDENT IT WAS DETERMINED THAT THE UNABLE TO PULL MEDICATIONS FROM THE SYSTEM. A TECHNICAL SUPPORT SPECIALIST TSS FOUND THAT ITEM IDENTIFIER 101223 WAS STOCKED IN THE CABINET BUT IT DID NOT MATCH WHAT WAS ON THE PATIENT PROFILE CAUSING IT NOT TO APPEAR. 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¿ MEDBANK TOWER AUX, THE MEDICATION WAS NOT SHOWING ON LIST, WHEN THE USER WAS TRYING TO PULL UP. THE CUSTOMER REPORTED THAT THE ISSUE OCCURRED WHEN THE USER WAS TRYING TO ISSUE MEDICATIONS TO A PATIENT. 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
    603634 BD PYXIS¿ MEDBANK TOWER AUX AUTOMATED DISPENSING CABINET BRY CAREFUSION 303, INC. 500004500001

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown