BEUDAMED
    FDA Adverse Event Summary report: N

    KNEE/ANKLE BRACE

    MDR report key: 2269510 · Received September 27, 2011

    Report

    Report Number
    2020737-2011-00012
    Date Received
    September 27, 2011
    Date of Event
    July 24, 2008
    Report Date
    September 27, 2011
    Manufacturer
    DJO GLOBAL
    Product Code
    ITQ
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RECEIPT OF LAWSUIT ON (B)(4) 2011 WAS FIRST NOTIFICATION OF COMPLAINT.

    Description of Event or Problem · 1

    COUNSEL STATES "PLAINTIFF WAS INJURED BY THE FOLLOWING PRODUCT: KNEE/ANKLE BRACE".

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KNEE/ANKLE BRACE ITQ DJO GLOBAL

    Patients

    Seq Age Sex Outcome Treatment
    1 Other