BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    FORCETRIAD

    MDR report key: 16378200 · Received February 15, 2023

    Report

    Report Number
    16378200
    Event Type
    No answer provided
    Date Received
    February 15, 2023
    Date of Event
    November 18, 2022
    Report Date
    November 18, 2022
    Manufacturer
    COVIDIEN
    Product Code
    GEI
    Report Source
    User Facility report
    Reporter Location
    WI
    Reporter Occupation
    RISK MANAGER
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    DURING USE OF TRIAD AN ERROR CODE REPEATEDLY CAME UP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1205633 FORCETRIAD ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES GEI COVIDIEN

    Patients

    Seq Age Sex Outcome Treatment
    1 16790 DA Female