BEUDAMED
    FDA Adverse Event Death Summary report: N

    EUFLEXXA PFS 20MG/2ML

    MDR report key: 20352735 · Received October 1, 2024

    Report

    Report Number
    MW5160437
    Event Type
    Death
    Date Received
    October 1, 2024
    Date of Event
    September 25, 2024
    Report Date
    September 30, 2024
    Manufacturer
    BIO-TECHNOLOGY GENERAL (ISRAEL) LTD.
    Product Code
    MOZ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    PT'S DAUGHTER REPORTED PT PASSED AWAY ON (B)(6) 2024. NO FURTHER INFO GIVEN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2016319 EUFLEXXA PFS 20MG/2ML ACID, HYALURONIC, INTRAARTICULAR MOZ BIO-TECHNOLOGY GENERAL (ISRAEL) LTD.

    Patients

    Seq Age Sex Outcome Treatment
    1 94 YR Female Death