BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNKNOWN ZIMMER NATURAL KNEE PATELLA

    MDR report key: 2133622 · Received June 16, 2011

    Report

    Report Number
    1822565-2011-01423
    Event Type
    Injury
    Date Received
    June 16, 2011
    Report Date
    May 20, 2011
    Manufacturer
    ZIMMER, INC.
    Product Code
    HTG
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    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 IS EXPERIENCING PAIN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNKNOWN ZIMMER NATURAL KNEE PATELLA KNEE PROSTHESIS HTG ZIMMER, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 Other