BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DO NOT KNOW

    MDR report key: 1033946 · Received April 24, 2008

    Report

    Report Number
    MW5006391
    Event Type
    Injury
    Date Received
    April 24, 2008
    Date of Event
    June 1, 1997
    Report Date
    April 24, 2008
    Manufacturer
    DON'T KNOW
    Product Code
    LZS
    Report Source
    Voluntary report
    Reporter Location
    AR, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND

    Narratives

    Description of Event or Problem · 1

    MY MOTHER, DAD, AUNT, HAD LASIK SURGERY, AND ALL OF THEM LOST THEIR EYE SIGHT. I THINK SOMETHING IS WRONG WITH THIS SURGERY. WE WENT TO A SPECIALIST AND THAT PLACE WAS FULL OF PEOPLE THAT HAD THAT SURGERY THAT WERE GOING BLIND. I THINK THIS SHOULD BE CHECKED INTO.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DO NOT KNOW EYE IMPLANTS LZS DON'T KNOW

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention HAVE TO LOOK UP LATER