BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LASIK

    MDR report key: 1812309 · Received August 17, 2010

    Report

    Report Number
    MW5017164
    Event Type
    Injury
    Date Received
    August 17, 2010
    Date of Event
    March 23, 2001
    Report Date
    August 17, 2010
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    I HAVE ALREADY REPORTED DR. (B)(6), DR. (B)(6). DR. (B)(6) WAS BANNED FROM PERFORMING LASIK SURGERY IN (B)(6). IF YOU CALL HIS OFFICE, THEY SAY HE'S DOING RESEARCH AND REFER YOU TO THE OTHER BUTCHER'S OFFICE, DR. (B)(6) WHO RUINED ME IN 2001. HE SETTLES WITH EVERYONE. HE SAID HE DID NO WRONGDOING, REPORTED MY OUTCOME TO THE FDA BECAUSE HE HAD NO IDEA WHY MY EYES WEREN'T ADHERING WELL TO THE LASIK PROCEDURE. I WASN'T A CANDIDATE AND HE WOULD NOT EXAMINE MY EYES. ANYHOW, HE HAD TOLD ME HE FILED THE FACT THAT I HAD A BAD OUTCOME -ALTHOUGH HE CLAIMED NOT TO HIS WRONGDOING. (B)(6). I HAVE BEEN TRYING TO HAVE DR. (B)(6)INVESTIGATED FOR YEARS. PLEASE HAVE THIS DONE.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 40 YR Required Intervention