BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    5385024

    MDR report key: 5385024 · Received January 22, 2016

    Report

    Report Number
    5385024
    Event Type
    Malfunction
    Date Received
    January 22, 2016
    Report Date
    December 1, 2015
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    MT, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    WHEN THE PRESSURE WIRE WAS PLUGGED IN WE NOTICED THE CATHETER DIP. THEY UNPLUGGED IT AND RE-PLUGGED IT IN BUT THE WAVE FORM JUST FLAT-LINED AND COULDN'T GET IT TO CHANGE. A SECOND ONE WAS PLUGGED IN BUT IT WOULD NOT ZERO, (0243 20064851 56) YET ANOTHER ONE WAS USED (3) IN ALL AND THE 3RD ONE USED WORKED FINE.

    Patients

    Seq Age Sex Outcome Treatment
    1 71 YR