BEUDAMED
    FDA Adverse Event Death Summary report: N

    DUROLANE 60 MG/3ML SYR (3=1)

    MDR report key: 16453231 · Received February 27, 2023

    Report

    Report Number
    MW5115269
    Event Type
    Death
    Date Received
    February 27, 2023
    Report Date
    February 22, 2023
    Manufacturer
    BIOVENTUS LLC
    Product Code
    MOZ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    PT PASSED AWAY ON (B)(6) 2023. INJECT 1 SYRINGE INTRA-ARTICULARLY INTO EACH KNEE ONCE BY PHYSICIAN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    845433 DUROLANE 60 MG/3ML SYR (3=1) ACID, HYALURONIC, INTRAARTICULAR MOZ BIOVENTUS LLC

    Patients

    Seq Age Sex Outcome Treatment
    1 Female Death