BEUDAMED
    FDA Adverse Event Other Summary report: N

    KNEE PROSTHESIS

    MDR report key: 39855 · Received September 27, 1996

    Report

    Report Number
    MW4001518
    Event Type
    Other
    Date Received
    September 27, 1996
    Date of Event
    August 7, 1996
    Report Date
    August 26, 1996
    Manufacturer
    BIOMET, INC.
    Product Code
    JWH
    Report Source
    Voluntary report
    Reporter Location
    AL, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    KNEE PROSTHESIS REMOVED DUE TO POSSIBLE DEFECT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KNEE PROSTHESIS Implant KNEE PROSTHESIS JWH BIOMET, INC. * 52251C

    Patients

    Seq Age Sex Outcome Treatment
    1 21 YR Other