BEUDAMED
    FDA Adverse Event Injury Summary report: N

    AMVISC PLUS

    MDR report key: 279363 · Received May 19, 2000

    Report

    Report Number
    MW1018989
    Event Type
    Injury
    Date Received
    May 19, 2000
    Date of Event
    May 10, 2000
    Report Date
    May 19, 2000
    Manufacturer
    CHIRON VISION CORP.
    Product Code
    LZP
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PTS WERE INJECTED WITH AMVISC PLUS RESULTING IN THE CLOUDING OF CORNEA.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AMVISC PLUS SODIUM HYALURONATE VISCOELASTIC LZP CHIRON VISION CORP. * B00208A

    Patients

    Seq Age Sex Outcome Treatment
    1 * Required Intervention