BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LASIK

    MDR report key: 1944031 · Received December 27, 2010

    Report

    Report Number
    MW5018731
    Event Type
    Injury
    Date Received
    December 27, 2010
    Date of Event
    April 22, 2000
    Report Date
    December 27, 2010
    Manufacturer
    UNK
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NC, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    THE LASIK PROCEDURE HAS LEFT ME WITH VERY LITTLE SIGHT IN THE RIGHT EYE AND AN ON GOING AND PROGRESSIVELY WORSENING LEFT EYE PROBLEMS. SCAR TISSUE SEEMS TO HAVE DEVELOPED IN THE RIGHT EYE OVER SIX YEARS AND AS PREVIOUSLY MENTIONED IS DOING THE SAME IN THE LEFT EYE. I'M TOLD BY EVERY OPHTHALMOLOGIST EYE SURGEON THAT THERE IS NO REMEDY.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 54 YR Required Intervention