BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ONLY HAD LASIK

    MDR report key: 2804257 · Received October 14, 2012

    Report

    Report Number
    MW5027340
    Event Type
    Injury
    Date Received
    October 14, 2012
    Date of Event
    October 10, 2010
    Report Date
    October 14, 2012
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    SUDDEN LARGE EYE FLOATERS AND SEVERE LIGHT FLASHES IN RIGHT EYE. DOCTOR CLAIMED I AM GETTING OLD. BUT I HAD LASIK SIX YEARS AGO, AND DID NOT HAVE ANY PROBLEMS UNTIL NOW.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 56 YR Required Intervention