BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LASIK

    MDR report key: 2021698 · Received March 12, 2011

    Report

    Report Number
    MW5019792
    Event Type
    Injury
    Date Received
    March 12, 2011
    Date of Event
    December 22, 2001
    Report Date
    March 12, 2011
    Manufacturer
    DD
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NC, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    SERIOUS SIDE EFFECTS AFTER LASIK. DR (B)(6). HE WAS TOO COCKY AND TOOK TOO MUCH OF MY CORNEA. OTHER DOCTORS SAY THAT HE SHOULDN'T HAVE DONE IT AND OFFERED OTHER TREATMENTS INSTEAD.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 32 YR Other| R