BEUDAMED
    FDA Adverse Event Death Summary report: N

    EUFLEXXA

    MDR report key: 7107542 · Received December 11, 2017

    Report

    Report Number
    MW5073893
    Event Type
    Death
    Date Received
    December 11, 2017
    Date of Event
    December 8, 2017
    Report Date
    December 8, 2017
    Manufacturer
    BIO-TECHNOLOGY GENERAL
    Product Code
    MOZ
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PATIENT IS DECEASED. UNILATERAL PRIMARY OSTEOARTHRITIS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    885052 EUFLEXXA ACID, HYALURONIC INTRAARTICULAR MOZ BIO-TECHNOLOGY GENERAL

    Patients

    Seq Age Sex Outcome Treatment
    1 63 YR Death