BEUDAMED
    FDA Adverse Event Death Summary report: N

    *

    MDR report key: 285079 · Received July 11, 2000

    Report

    Report Number
    285079
    Event Type
    Death
    Date Received
    July 11, 2000
    Date of Event
    June 20, 2000
    Report Date
    July 3, 2000
    Manufacturer
    ABBOTT LABORATORIES
    Product Code
    DYG
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    TX, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    PT WAS A POST-OP. HAD A SURGICALLY PLACED SWAN GANZ CATHETER IN PLACE. CATHETER WORKING WELL BEFORE AND HAD GOOD READINGS. USED FOR READINGS EVERY 2 HRS. AT AM WEDGING, RESULTS OBTAINED. APPROX 2 MINUTES LATER, PT BEGAN COUGHING UP BLOOD. PT SUBSEQUENTLY CODED AND EXPIRED. BIOMEDICAL ENGINEERING RECEIVED OCCURRENCE REPORT 6/30/2000. MEDICAL EXAMINER IN POSSESSION OF CATHETER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * THERMODILUTION CATHETER DYG ABBOTT LABORATORIES 41239-04-01 *

    Patients

    Seq Age Sex Outcome Treatment
    1 86 YR Death