BEUDAMED
    FDA Adverse Event Injury Summary report: N

    KNEE IMPLANT

    MDR report key: 2161395 · Received July 13, 2011

    Report

    Report Number
    1020279-2011-00252
    Event Type
    Injury
    Date Received
    July 13, 2011
    Date of Event
    June 15, 2011
    Report Date
    July 12, 2011
    Manufacturer
    SMTIH & NEPHEW, INC. ORTHOPAEDIC DIVISION
    Product Code
    JWH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WV, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT HAS BEEN REPORTED THAT THE PATIENT'S KNEE DISLOCATED. THE PATIENT WAS ADMITTED TO THE HOSPITAL AND PUT UNDER ANESTHESIA TO MANIPULATE THE KNEE. PRODUCT IS NOT AVAILABLE FOR RETURN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KNEE IMPLANT FEMORAL JWH SMTIH & NEPHEW, INC. ORTHOPAEDIC DIVISION

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| R