BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LASIK

    MDR report key: 4231608 · Received November 2, 2014

    Report

    Report Number
    MW5038949
    Event Type
    Injury
    Date Received
    November 2, 2014
    Date of Event
    August 2, 2003
    Report Date
    November 2, 2014
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    LASIK SURGERY WENT WRONG. BACK TO CONTACTS AND CAN'T SEE WITH GLASSES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    700896 LASIK LASIK LZS

    Patients

    Seq Age Sex Outcome Treatment
    1