BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LASIK

    MDR report key: 2190688 · Received July 30, 2011

    Report

    Report Number
    MW5021567
    Event Type
    Injury
    Date Received
    July 30, 2011
    Date of Event
    July 23, 2011
    Report Date
    July 30, 2011
    Manufacturer
    LASIK
    Product Code
    LZS
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IL, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    BOTCHED LASIK SURGERY LEADS TO HALOS, STARBURSTS, DRY EYE, PAIN, DEPRESSION, SUICIDAL THOUGHTS, AND DISCOMFORT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 25 YR Required Intervention