BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SYNVISC HYLAN G-F20

    MDR report key: 21020982 · Received December 26, 2024

    Report

    Report Number
    MW5163970
    Event Type
    Malfunction
    Date Received
    December 26, 2024
    Date of Event
    December 17, 2024
    Report Date
    December 19, 2024
    Manufacturer
    GENZYME CORPORATION
    Product Code
    MOZ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    WA, US
    Reporter Occupation
    PHYSICAL THERAPIST
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    FINGER FLANGE OFF SYRINGE, BROKE DURING APPLICATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2429183 SYNVISC HYLAN G-F20 ACID, HYALURONIC, INTRAARTICULAR MOZ GENZYME CORPORATION 002401 ERSL028

    Patients

    Seq Age Sex Outcome Treatment
    1 79 YR Female