BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BD ALARIS PUMP TUBING

    MDR report key: 21422262 · Received February 20, 2025

    Report

    Report Number
    MW5166546
    Event Type
    Injury
    Date Received
    February 20, 2025
    Date of Event
    February 11, 2025
    Report Date
    February 14, 2025
    Manufacturer
    CAREFUSION 2200, INC.
    Product Code
    FPA
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    WHEN PUMP CHANNEL WAS OPENED, TUBING IN BOTTOM HALF OF CHANNEL SPLIT FROM TOP PART OF TUBING TO RITUXAN. RITUXAN WAS FREE FLOWING FROM REMAINING TUBING ABOVE CHANNEL AND ONTO THE FLOOR. UNABLE TO CLAMP TUBING WITH CLAMP ON THE TUBING IN CHANNEL SO CHANNEL WAS CLOSED TO PREVENT FURTHER SPILL. NO RITUXAN GOT ONTO PATIENT. SPILL KIT WAS USED TO CLEAN SPILL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1045757 BD ALARIS PUMP TUBING SET, ADMINISTRATION, INTRAVASCULAR FPA CAREFUSION 2200, INC. 24085390

    Patients

    Seq Age Sex Outcome Treatment
    1 Male TUBING- LOT #: 24115025