BEUDAMED
    FDA Adverse Event Summary report: N

    ULTRASONIC CURVED SHEARS

    MDR report key: 3040029 · Received April 2, 2013

    Report

    Report Number
    MW5029612
    Date Received
    April 2, 2013
    Date of Event
    February 2, 2013
    Report Date
    March 21, 2013
    Manufacturer
    ETHICON ENDO - SURGERY INC.
    Product Code
    LFL
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MD, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DURING PT'S RIGHT HEMITHYROIDECTOMY HARMONIC FOCUS WAS DYSFUNCTIONAL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    135289 ULTRASONIC CURVED SHEARS NONE LFL ETHICON ENDO - SURGERY INC. 2219192

    Patients

    Seq Age Sex Outcome Treatment
    1 64 YR Required Intervention