BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NA

    MDR report key: 1680285 · Received May 5, 2010

    Report

    Report Number
    MW5015849
    Event Type
    Injury
    Date Received
    May 5, 2010
    Report Date
    May 5, 2010
    Manufacturer
    NA
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    GA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    SEVERE AND PAINFUL DRY EYES, 5 YEARS AFTER LASIK SURGERY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NA LASIK LZS NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 Other