BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STRYKER

    MDR report key: 1061852 · Received June 17, 2008

    Report

    Report Number
    MW5007325
    Event Type
    Malfunction
    Date Received
    June 17, 2008
    Date of Event
    June 4, 2008
    Report Date
    June 5, 2008
    Manufacturer
    STRYKER
    Product Code
    DZH
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE HEAD OF THE SAGGITTAL SAW CAME APART ON THE FIELD WHILE USING ON THE PT'S FOOT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRYKER SAGGITAL SAW DZH STRYKER COMMAND II

    Patients

    Seq Age Sex Outcome Treatment
    1