BEUDAMED
    FDA Adverse Event Other Summary report: N

    DUROLANE 60 MG/3ML SYRINGE

    MDR report key: 23053574 · Received September 15, 2025

    Report

    Report Number
    MW5176065
    Event Type
    Other
    Date Received
    September 15, 2025
    Date of Event
    September 8, 2025
    Report Date
    September 10, 2025
    Manufacturer
    BIOVENTUS LLC
    Product Code
    MOZ
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    PATIENT REPORTED BEING ADMITTED TO THE HOSPITAL ON (B)(6) 20255 DUE TO PRIOR AMPUTATION OF LEG. NO ADDITIONAL INFO PROVIDED. PATIENT DOES NOT CONSENT TO BEING CONTACTED. REPORTER CONSENTS FOR MANUFACTURER FOLLOW-UP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2640312 DUROLANE 60 MG/3ML SYRINGE ACID, HYALURONIC, INTRAARTICULAR MOZ BIOVENTUS LLC

    Patients

    Seq Age Sex Outcome Treatment
    1 75 YR Male