BEUDAMED
    FDA Adverse Event Death Summary report: N

    SWAN GANZ

    MDR report key: 1695562 · Received May 18, 2010

    Report

    Report Number
    MW5015983
    Event Type
    Death
    Date Received
    May 18, 2010
    Date of Event
    March 18, 2010
    Report Date
    April 5, 2010
    Manufacturer
    EDWARDS LIFESCIENCES TECHNOLOGY SARL
    Product Code
    DYG
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    RUPTURED PULMONARY ARTERY DURING RIGHT HEART CATHETER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SWAN GANZ SWAN GANZ TD CATHETER 1.5 ML CAP .131F7 DYG EDWARDS LIFESCIENCES TECHNOLOGY SARL

    Patients

    Seq Age Sex Outcome Treatment
    1 88 YR Death