BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ABBOTT

    MDR report key: 225425 · Received May 25, 1999

    Report

    Report Number
    MW1016411
    Event Type
    Injury
    Date Received
    May 25, 1999
    Date of Event
    May 25, 1999
    Report Date
    May 25, 1999
    Manufacturer
    ABBOTT LABORATORIES, INC.
    Product Code
    FPA
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    WI, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    TUBING WOULD NOT RUN ON PUMP. TRIED 3 PUMPS WITHOUT IT RUNNING PROPERLY. PT WAS CRITICAL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ABBOTT NITROGLYCERINE SET FPA ABBOTT LABORATORIES, INC. * 848041Y

    Patients

    Seq Age Sex Outcome Treatment
    1 * Life Threatening