BEUDAMED
    FDA Adverse Event Injury Summary report: N

    VEGA TOTAL KNEE

    MDR report key: 7464218 · Received April 25, 2018

    Report

    Report Number
    MW5076757
    Event Type
    Injury
    Date Received
    April 25, 2018
    Date of Event
    February 5, 2018
    Report Date
    April 17, 2018
    Manufacturer
    AESCULAP AG / B. BRAUN
    Product Code
    JWH
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    NO INFORMATION

    Narratives

    Description of Event or Problem · 1

    LOOSENING TIBIA AND FEMUR STOOD OUT FEMUR FIRST.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    304524 VEGA TOTAL KNEE PROSTHESIS, KNEE JWH AESCULAP AG / B. BRAUN

    Patients

    Seq Age Sex Outcome Treatment
    1 67 YR Required Intervention