BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SWAN-GANZ CONTINUOUS CARDIAC OUTPUT CATHETER

    MDR report key: 1040665 · Received May 7, 2008

    Report

    Report Number
    6000002-2008-07071
    Event Type
    Malfunction
    Date Received
    May 7, 2008
    Date of Event
    February 2, 2008
    Report Date
    April 14, 2008
    Manufacturer
    EDWARDS LIFESCIENCES, PR
    Product Code
    DYG
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    DEVICE NOT RETURNED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE CARDIAC INDEX MONITOR READING WAS 7.2 AND A MANUAL CARDIAC INDEX BOLUS WAS PERFORMED FOR A RESULT OF 4.2. NO PATIENT COMPLICATIONS WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SWAN-GANZ CONTINUOUS CARDIAC OUTPUT CATHETER CONTINUOUS CARDIAC OUTPUT CATHETER DYG EDWARDS LIFESCIENCES, PR 746HF8 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Other