BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LASIK

    MDR report key: 4182076 · Received October 9, 2014

    Report

    Report Number
    MW5038636
    Event Type
    Injury
    Date Received
    October 9, 2014
    Date of Event
    September 10, 2009
    Report Date
    October 9, 2014
    Product Code
    LZS
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    LASIK EYE SURGERY. NIGHT VISION PROBLEMS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    634684 LASIK LASIK LZS

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR Disability