BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TURBOHAWK

    MDR report key: 3861369 · Received May 20, 2014

    Report

    Report Number
    3861369
    Event Type
    Malfunction
    Date Received
    May 20, 2014
    Date of Event
    January 28, 2014
    Report Date
    May 20, 2014
    Manufacturer
    COVIDIEN
    Product Code
    MCW
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    IL, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    298645 TURBOHAWK CATHETER, PERIPHERAL, ATHERECTOMY MCW COVIDIEN * 9831693

    Patients

    Seq Age Sex Outcome Treatment
    1 *