BEUDAMED
    FDA Adverse Event Death Summary report: N

    SYNVISC PFS 8MG/ML (3X2ML)

    MDR report key: 12049314 · Received June 22, 2021

    Report

    Report Number
    MW5102014
    Event Type
    Death
    Date Received
    June 22, 2021
    Date of Event
    June 11, 2021
    Report Date
    June 17, 2021
    Manufacturer
    GENZYME CORPORATION
    Product Code
    MOZ
    UDI-DI
    58468009001
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    003

    Narratives

    Description of Event or Problem · 1

    PT PASSED AWAY ON (B)(6) 2021.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    935737 SYNVISC PFS 8MG/ML (3X2ML) ACID, HYALURONIC, INTRAARTICULAR MOZ GENZYME CORPORATION 58468009001

    Patients

    Seq Age Sex Outcome Treatment
    1 90 YR Death