BEUDAMED
    FDA Adverse Event Death Summary report: N

    DUROLANE

    MDR report key: 8816878 · Received July 22, 2019

    Report

    Report Number
    MW5088275
    Event Type
    Death
    Date Received
    July 22, 2019
    Report Date
    July 18, 2019
    Manufacturer
    BIOVENTUS LLC
    Product Code
    MOZ
    UDI-DI
    89130202001
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PT'S DAUGHTER REPORTED THAT THE PT HAD PASSED AWAY IN (B)(6) 2019. EXACT DATE OF DEATH IS UNK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    603945 DUROLANE ACID, HYALURONIC, INTRAARTICULAR MOZ BIOVENTUS LLC 15862 89130202001

    Patients

    Seq Age Sex Outcome Treatment
    1 Death