BEUDAMED
    FDA Adverse Event Death Summary report: N

    SYNVISC PFS 8MG/ML (3X2ML)

    MDR report key: 12216858 · Received July 22, 2021

    Report

    Report Number
    MW5102720
    Event Type
    Death
    Date Received
    July 22, 2021
    Date of Event
    May 13, 2021
    Manufacturer
    GENZYME CORPORATION
    Product Code
    MOZ
    UDI-DI
    58468009001
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PT DECEASED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1112562 SYNVISC PFS 8MG/ML (3X2ML) ACID, HYALURONIC, INTRAARTICULAR MOZ GENZYME CORPORATION 58468009001

    Patients

    Seq Age Sex Outcome Treatment
    1 92 YR Death