BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SYNVISC-ONE INJECTION

    MDR report key: 24133773 · Received January 21, 2026

    Report

    Report Number
    MW5182568
    Event Type
    Malfunction
    Date Received
    January 21, 2026
    Report Date
    January 15, 2026
    Manufacturer
    GENZYME CORPORATION
    Product Code
    MOZ
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    KS, US
    Reporter Occupation
    PHARMACIST
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    DESCRIBE EVENT, PROBLEM, OR PRODUCT USE ERROR: HUB FELL OFF OF INJECTION WHILST TRYING TO SCREW ON NEEDLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    202963 SYNVISC-ONE INJECTION ACID, HYALURONIC, INTRAARTICULAR MOZ GENZYME CORPORATION FRSLB26

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown