BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    COVIDIEN

    MDR report key: 2464226 · Received February 8, 2012

    Report

    Report Number
    2464226
    Event Type
    Malfunction
    Date Received
    February 8, 2012
    Date of Event
    February 2, 2012
    Report Date
    February 8, 2012
    Manufacturer
    COVIDIEN
    Product Code
    FZP
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MA, US

    Narratives

    Description of Event or Problem · 1

    ENDO CLIP APPLIER WAS OPENED FOR CASE. ITEM DID NOT WORK - NOT USED ON PATIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 COVIDIEN CLIP APPLIER FZP COVIDIEN 10MM N1A0327

    Patients

    Seq Age Sex Outcome Treatment
    1 *