BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LASIK SURGERY

    MDR report key: 1040883 · Received May 9, 2008

    Report

    Report Number
    MW5006802
    Event Type
    Injury
    Date Received
    May 9, 2008
    Date of Event
    April 20, 2007
    Report Date
    May 9, 2008
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    AL, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    MY CORNEA WAS TORN IN SEVERAL PLACES WHEN THE DOCTOR WAS ATTEMPTING TO CREATE A FLAP FOR MY LASIK PROCEDURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LASIK SURGERY NONE LZS

    Patients

    Seq Age Sex Outcome Treatment
    1 Other