BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ABC PROBE

    MDR report key: 1001420 · Received January 25, 2008

    Report

    Report Number
    1001420
    Event Type
    Malfunction
    Date Received
    January 25, 2008
    Date of Event
    January 23, 2008
    Report Date
    January 25, 2008
    Manufacturer
    CONMED ELECTROSURGERY
    Product Code
    GEI
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    UT, US

    Narratives

    Description of Event or Problem · 1

    WHEN THE CONMED ABC PROBE WAS WIPED OFF, THE SHARP/NEEDLE PULLED OUT OF THE PROBE TIP. THE PROBE WAS NOT USED AFTERWARDS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ABC PROBE PROBE, ARGON BEAM COAGULATION GEI CONMED ELECTROSURGERY 160656 0706061

    Patients

    Seq Age Sex Outcome Treatment
    1 74 YR