BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LASIK

    MDR report key: 1040324 · Received May 7, 2008

    Report

    Report Number
    MW5006775
    Event Type
    Injury
    Date Received
    May 7, 2008
    Date of Event
    December 21, 2007
    Report Date
    May 7, 2008
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    UT, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I RECEIVED LASER EYE SURGERY IN LATE 2007. WITHIN 3 MONTHS, IT WAS CLEAR THAT I NEED TO HAVE MY RIGHT EYE TREATED AGAIN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LASIK LASER EYE SURGERY LZS

    Patients

    Seq Age Sex Outcome Treatment
    1 33 YR Other