BEUDAMED
    FDA Adverse Event Death Summary report: N

    SYNVISC ONE

    MDR report key: 15454802 · Received September 19, 2022

    Report

    Report Number
    MW5112117
    Event Type
    Death
    Date Received
    September 19, 2022
    Date of Event
    September 12, 2022
    Report Date
    September 14, 2022
    Manufacturer
    GENZYME CORPORATION
    Product Code
    MOZ
    UDI-DI
    58468009003
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    AS, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    PT'S WIFE REPORTS THAT PT DIED ON (B)(6) 2022. NO CAUSE OF DEATH GIVEN BY THE REPORTER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    125985 SYNVISC ONE ACID, HYALURONIC, INTRAARTICULAR MOZ GENZYME CORPORATION 58468009003

    Patients

    Seq Age Sex Outcome Treatment
    1 79 YR Male Death