BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNKNOWN ZIMMER SEGMENTAL KNEE

    MDR report key: 2890764 · Received December 21, 2012

    Report

    Report Number
    1822565-2012-02619
    Event Type
    Injury
    Date Received
    December 21, 2012
    Date of Event
    November 20, 2012
    Report Date
    November 30, 2012
    Manufacturer
    ZIMMER INC
    Product Code
    JWH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THIS REPORT WILL BE AMENDED WHEN OUR INVESTIGATION IS COMPLETE.

    Description of Event or Problem · 1

    IT IS REPORTED THAT THE PATIENT WAS REVISED DUE TO INFECTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNKNOWN ZIMMER SEGMENTAL KNEE KNEE PROSTHESIS JWH ZIMMER INC

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR Required Intervention