BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ETHICON HARMONIC SCAPEL

    MDR report key: 1033384 · Received April 23, 2008

    Report

    Report Number
    MW5006363
    Event Type
    Malfunction
    Date Received
    April 23, 2008
    Date of Event
    April 22, 2008
    Report Date
    April 23, 2008
    Manufacturer
    ETHICON CORP HEADQUARTERS
    Product Code
    LFL
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    PRODUCT WOULD NOT FIRE DURING THE PROCEDURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ETHICON HARMONIC SCAPEL HARMONIC ACE LFL ETHICON CORP HEADQUARTERS ACE E4KP5W

    Patients

    Seq Age Sex Outcome Treatment
    1