BEUDAMED
    FDA Adverse Event Injury Summary report: N

    WRIGHT MEDICAL TECH

    MDR report key: 208733 · Received September 2, 1997

    Report

    Report Number
    208733
    Event Type
    Injury
    Date Received
    September 2, 1997
    Date of Event
    April 1, 1997
    Report Date
    May 8, 1997
    Manufacturer
    WRIGHT MEDICAL
    Product Code
    KRP
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    PAINFUL LEFT TOTAL KNEE ARTHROPLASTY SECONDARY TO LOOSE FEMORAL AND TIBIAL COMPONENTS. DISRUPTION EXTENSOR MECHANISM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 WRIGHT MEDICAL TECH Implant LEFT TOTAL KNEE KRP WRIGHT MEDICAL * 104A004908

    Patients

    Seq Age Sex Outcome Treatment
    1 57 YR Required Intervention