BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BD ALARIS

    MDR report key: 23295825 · Received October 15, 2025

    Report

    Report Number
    MW5177346
    Event Type
    Injury
    Date Received
    October 15, 2025
    Date of Event
    September 16, 2025
    Report Date
    October 9, 2025
    Manufacturer
    CAREFUSION 303, INC.
    Product Code
    FRN
    Report Source
    Voluntary report
    Reporter Location
    CO, US
    Reporter Occupation
    PHARMACIST
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    INFUSION PUMP WAS PROGRAMMED TO RUN 20 ML/HR FOR 23.5 HOUR METHOTREXATE INFUSION. INFUSION ALARMED EMPTY AFTER 4 HOURS. PUMP RAN WRONG RATE AND/OR RAN AT GRAVITY, DESPITE THE TUBING BEING INSERTED CORRECTLY AND THE PUMP BEING PROGRAMMED CORRECTLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2470986 BD ALARIS PUMP, INFUSION FRN CAREFUSION 303, INC. 8100

    Patients

    Seq Age Sex Outcome Treatment
    1 10 YR Male Hospitalization