BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NA

    MDR report key: 1630776 · Received March 8, 2010

    Report

    Report Number
    MW5015089
    Event Type
    Injury
    Date Received
    March 8, 2010
    Date of Event
    October 16, 2005
    Report Date
    March 8, 2010
    Manufacturer
    NA
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    GA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    MY LEFT EYE HAD BAD CORNEA SCARRING AND I NEED A CORNEA TRANSPLANT WHICH COSTS (B) (6) THAT I DON'T HAVE. I HAVE TO CLOSE MY LEFT EYE WHILE I SEE WITH MY RIGHT ONE OR THE BAD SIGHT OVERLAPS WITH MY RIGHT EYE. I NOW HAVE ONE GOOD EYE ... AND GLASSES DON'T HELP. CONTACTS HURT AFTER 4 HOURS IN MY LEFT EYE, SO I CAN'T WEAR THEM ALL DAY. ALSO MY LEFT EYE IS 20/100 WITH DOUBLE VISION AND VERY BAD LIGHT STREAKS AT NIGHT. I JUST WANT MY LEFT EYE TAKEN OUT; IT BOTHERS ME WHEN I TRY TO SEE WITH MY OTHER 20/30 RIGHT EYE. I GOT LAID OFF TWO MONTHS AGO, AND IT PROBABLY WILL BE HARDER WITH ONE EYE TO KEEP ANY DECENT JOB. I HAD FOUR OPERATIONS -ENHANCEMENTS- THAT CAUSED TRAUMA TO MY LEFT EYE AND STARTED (B) (6) SIMPLEX WHICH CAUSED DAMAGE TO MY LEFT EYE. THE PLACE WHERE I HAD OPERATIONS WILL NOT HELP ME AT ALL WITH MONEY BECAUSE THEY SAY I CAN'T PROVE THAT THE LASERS CAUSED THE VIRUS. I AM VERY MAD, BUT CAN'T DO ANYTHING ABOUT IT. BY THE WAY, I DID NOT HAVE (B) (6) BEFORE THE OPERATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NA LASER LZS NA NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 48 YR Other| R