BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SYNVISC 20MG

    MDR report key: 24547550 · Received March 9, 2026

    Report

    Report Number
    MW5184913
    Event Type
    Malfunction
    Date Received
    March 9, 2026
    Report Date
    March 3, 2026
    Manufacturer
    SANOFI GENZYME CORP.
    Product Code
    MOZ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    US
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    REPORTER STATED THAT THE PATIENT HAD TRIED AND FAILED SYNVISC. THE PATIENT HAS STATED THAT THE MEDICATION WAS NOT WORKING FOR THEM. REPORTED BY HCP, THEY DID CONSENT TO FOLLOW UP. (B)(6), ALL AVAILABLE INFORMATION IS PROVIDED IN THIS REPORT NO FURTHER CLARIFICATION IS AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    614942 SYNVISC 20MG ACID, HYALURONIC, INTRAARTICULAR MOZ SANOFI GENZYME CORP.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown