BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TURON SHOULDER

    MDR report key: 1760828 · Received July 14, 2010

    Report

    Report Number
    1644408-2010-00371
    Event Type
    Malfunction
    Date Received
    July 14, 2010
    Date of Event
    June 14, 2010
    Report Date
    June 14, 2010
    Manufacturer
    ENCORE MEDICAL, L.P.
    Product Code
    LXH
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    TURON HEAD INSTRUMENT BROKE DURING TRIALS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TURON SHOULDER HUMERAL INSTRUMENT, TRIAL LXH ENCORE MEDICAL, L.P. UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1