BEUDAMED
    FDA Adverse Event Death Summary report: N

    SWAN GANZ CATHETER

    MDR report key: 31715 · Received March 2, 1996

    Report

    Report Number
    31715
    Event Type
    Death
    Date Received
    March 2, 1996
    Date of Event
    January 16, 1996
    Report Date
    February 26, 1996
    Manufacturer
    EDWARDS CVS DIV. BAXTER HEALTHCARE CORP.
    Product Code
    DYG
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    MN, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    CATHETER WAS PLACED WITHOUT PROBLEM. GOOD PA WAVE FORM. CATHETER WAS FLOATED TO WEDGE POSITION. BALLOON WAS DEFLATED. PATIENT DEVELOPED HEMOPTYSIS. NO AGGRESSIVE RESUSCITATION DUE TO DNR/DNI STATUS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SWAN GANZ CATHETER CATHETER DYG EDWARDS CVS DIV. BAXTER HEALTHCARE CORP. 131HF-7PAK

    Patients

    Seq Age Sex Outcome Treatment
    1 75 YR Death