BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LASIK SURGERY

    MDR report key: 1190204 · Received October 6, 2008

    Report

    Report Number
    MW5008545
    Event Type
    Injury
    Date Received
    October 6, 2008
    Date of Event
    October 6, 2008
    Report Date
    October 6, 2008
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    ECTASIA IN BOTH EYES DUE TO LASIK SURGERY.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention