BEUDAMED
    FDA Adverse Event Injury Summary report: N

    N/A

    MDR report key: 2163552 · Received July 11, 2011

    Report

    Report Number
    MW5021316
    Event Type
    Injury
    Date Received
    July 11, 2011
    Report Date
    July 11, 2011
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CO, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I HAD LASIK AND NOW HAVE ECTASIA. MY VISION CHANGES EVERY SIX MONTHS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 N/A LASIK LZS

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention