BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CURITY

    MDR report key: 2926414 · Received January 21, 2013

    Report

    Report Number
    2926414
    Event Type
    Malfunction
    Date Received
    January 21, 2013
    Date of Event
    January 8, 2013
    Report Date
    January 21, 2013
    Manufacturer
    COVIDEN
    Product Code
    GDW
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    RI, US

    Narratives

    Description of Event or Problem · 1

    NEW STAPLE REMOVAL KIT DOES NOT WORK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    28607 CURITY STAPLE, IMPLANTABLE GDW COVIDEN * 224388464X

    Patients

    Seq Age Sex Outcome Treatment
    1 2 YR