BEUDAMED
    FDA Adverse Event Injury Summary report: N

    KNEE IMPLANT

    MDR report key: 2143197 · Received June 28, 2011

    Report

    Report Number
    1020279-2011-00228
    Event Type
    Injury
    Date Received
    June 28, 2011
    Date of Event
    June 6, 2011
    Report Date
    June 28, 2011
    Manufacturer
    SMTIH & NEPHEW, INC. ORTHOPAEDIC DIVISION
    Product Code
    JWH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT HAS BEEN REPORTED THAT A REVISION SURGERY WAS PERFORMED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| R