BEUDAMED
    FDA Adverse Event Other Summary report: N

    BD ALARIS PUMP MODULE INFUSION SET

    MDR report key: 25069096 · Received May 4, 2026

    Report

    Report Number
    MW5187570
    Event Type
    Other
    Date Received
    May 4, 2026
    Date of Event
    April 24, 2026
    Report Date
    April 29, 2026
    Manufacturer
    BD / BECTON, DICKINSON AND COMPANY / CAREFUSION 2200, INC.
    Product Code
    FPA
    Report Source
    Voluntary report
    Reporter Location
    SC, US
    Reporter Occupation
    UNKNOWN
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    THE INTRAVENOUS TUBING SET CAME APART AFTER SPIKING THE MAGNESIUM BAG, SPILLED MAGNESIUM ON THE FLOOR. TUBING AND MAGNESIUM HAD TO BE THROWN AWAY AND REPLACED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    470912 BD ALARIS PUMP MODULE INFUSION SET SET, ADMINISTRATION, INTRAVASCULAR FPA BD / BECTON, DICKINSON AND COMPANY / CAREFUSION 2200, INC. 26025231

    Patients

    Seq Age Sex Outcome Treatment
    1 78 YR Female Other