BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DOW CORNING WRIGHT

    MDR report key: 116770 · Received August 28, 1997

    Report

    Report Number
    116770
    Event Type
    Injury
    Date Received
    August 28, 1997
    Date of Event
    August 21, 1997
    Report Date
    August 28, 1997
    Manufacturer
    WRIGHT MEDICAL TECHNOLOGIES
    Product Code
    JWH
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    KS, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    CHIEF COMPLAINT: LEFT KNEE PAIN, ACHE AND SORENESS NOTED WHILE TWISTING. DOES NOT HAVE GOOD FLEXION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DOW CORNING WRIGHT Implant TOTAL CONDYLAR TIBIAL INSERT JWH WRIGHT MEDICAL TECHNOLOGIES * 011M553420

    Patients

    Seq Age Sex Outcome Treatment
    1 71 YR Required Intervention