BEUDAMED
    FDA Adverse Event Other Summary report: N

    ALCON

    MDR report key: 249430 · Received November 4, 1999

    Report

    Report Number
    MW1017522
    Event Type
    Other
    Date Received
    November 4, 1999
    Date of Event
    October 29, 1999
    Report Date
    November 3, 1999
    Manufacturer
    ALCON LABORATORIES
    Product Code
    GAW
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    LA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    AFTER CATARACT SURGERY WAS COMPLETE, THE SURGEON INFORMED THE NURSES IN THE ROOM THAT A CORNEAL BURN HAD RESULTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ALCON PHACO GAW ALCON LABORATORIES LEGACY NA

    Patients

    Seq Age Sex Outcome Treatment
    1 62 YR Other