BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GREENLIGHT ADDSTAT

    MDR report key: 1913305 · Received November 11, 2010

    Report

    Report Number
    2937094-2010-01021
    Event Type
    Malfunction
    Date Received
    November 11, 2010
    Date of Event
    September 20, 2010
    Report Date
    October 14, 2010
    Manufacturer
    AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY
    Product Code
    GEX
    PMA / PMN Number
    K062719
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY THE CUSTOMER THAT ON (B)(6) 2010, THE FIBER TIP SUDDENLY MELTED AT 41,466 JOULES. ALSO, IT WAS REPORTED THAT THE FIBER TIP WAS NOT BURIED IN THE TISSUE WHEN IT MELTED. THE DEVICE WAS NOT RETURNED FOR EVAL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GREENLIGHT ADDSTAT SURGICAL FIBER GEX AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY NA 022H

    Patients

    Seq Age Sex Outcome Treatment
    1 Other