BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CONMED CORPORATION

    MDR report key: 418310 · Received September 19, 2002

    Report

    Report Number
    1720159-2002-00122
    Event Type
    Malfunction
    Date Received
    September 19, 2002
    Date of Event
    August 22, 2002
    Report Date
    August 22, 2002
    Manufacturer
    CONMED ELECTROSURGERY
    Product Code
    GEI
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THREE ABC PROBES DURING ONE PROCEDURE BECAME EXTREMELY HOT ON THE TIP AND STARTED TO MELT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CONMED CORPORATION ABC LAPAROSCOPIC HANDPIECE GEI CONMED ELECTROSURGERY ABC PROBE 020228-1

    Patients

    Seq Age Sex Outcome Treatment
    1 NA