BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MISHA® KNEE SYSTEM, SMALL, RIGHT

    MDR report key: 24114723 · Received January 20, 2026

    Report

    Report Number
    24114723
    Event Type
    Malfunction
    Date Received
    January 20, 2026
    Date of Event
    December 11, 2025
    Report Date
    December 16, 2025
    Manufacturer
    MOXIMED, INC.
    Product Code
    QVV
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA
    Reporter Occupation
    RISK MANAGER
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    MD WAS HANDLING IMPLANT WHEN IMPLANT BROKE. IMPLANT WAS PLACED OFF STERILE FIELD AND NEW IMPLANT WAS OPENED AND USED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    178514 MISHA® KNEE SYSTEM, SMALL, RIGHT MEDIAL KNEE IMPLANTED SHOCK ABSORBER QVV MOXIMED, INC. 2-1002 25042201

    Patients

    Seq Age Sex Outcome Treatment
    1 46 YR Male