BEUDAMED
    FDA Adverse Event Other Summary report: N

    LIGASURE-LONG CURVED

    MDR report key: 1904279 · Received November 17, 2010

    Report

    Report Number
    MW5018245
    Event Type
    Other
    Date Received
    November 17, 2010
    Date of Event
    November 3, 2010
    Report Date
    November 8, 2010
    Manufacturer
    VALLEY LAB
    Product Code
    GEI
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    SURGEON COULD NOT GET THIS FOOT ACTIVATED HANDPIECE TO FUNCTION CORRECTLY. PROPER CAUTERY COULD NOT BE ESTABLISHED AND MACHINE WOULD READ TO REGRASP TISSUE SAMPLE. STAFF DID OBTAIN A SECOND MACHINE AND A SECOND HANDPIECE TYPE. THE SURGEON USING THE EQUIPMENT HAS BEEN USING THIS EQUIPMENT/TECHNOLOGY FOR YEARS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIGASURE-LONG CURVED GEI VALLEY LAB 157292

    Patients

    Seq Age Sex Outcome Treatment
    1 64 YR