BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COVIDIEN

    MDR report key: 3798946 · Received May 6, 2014

    Report

    Report Number
    3798946
    Event Type
    Malfunction
    Date Received
    May 6, 2014
    Date of Event
    May 5, 2014
    Report Date
    May 6, 2014
    Manufacturer
    COVIDIEN
    Product Code
    GEI
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    WHEN ATTEMPTING TO OPERATE THE INSTRUMENT, THE GRASPING TIP OF THE INSTRUMENT WOULD NOT OPEN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    271603 COVIDIEN ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES GEI COVIDIEN * 40510154X

    Patients

    Seq Age Sex Outcome Treatment
    1 23 YR