BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ABBOTT

    MDR report key: 272394 · Received April 4, 2000

    Report

    Report Number
    MW1018568
    Event Type
    Malfunction
    Date Received
    April 4, 2000
    Date of Event
    March 9, 2000
    Report Date
    March 30, 2000
    Manufacturer
    ABBOTT LABORATORIES
    Product Code
    DYG
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    VA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    SWAN-GANZ THERMODILUTION CATHETER MALFUNCTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ABBOTT THERMO DILUTION CATHETER DYG ABBOTT LABORATORIES * *

    Patients

    Seq Age Sex Outcome Treatment
    1 61 YR