BEUDAMED
    FDA Adverse Event Injury Summary report: N

    INTRALASE FS2

    MDR report key: 3872724 · Received June 13, 2014

    Report

    Report Number
    3006695864-2014-00304
    Event Type
    Injury
    Date Received
    June 13, 2014
    Date of Event
    February 5, 2014
    Report Date
    February 7, 2014
    Manufacturer
    ABBOTT MEDICAL OPTICS
    Product Code
    HNO
    PMA / PMN Number
    K060372
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THE CLINIC IS REPORTING THIS ADVERSE EVENT ONLY AND DID NOT REQUEST OR REQUIRE FIELD SERVICE OR CLINICAL SUPPORT. ALL PERTINENT INFORMATION AVAILABLE TO ABBOTT MEDICAL OPTICS HAS BEEN SUBMITTED. PLACEHOLDER.

    Description of Event or Problem · 1

    THE CLINIC REPORTED THAT A LASER VISION CORRECTION PATIENT PRESENTED COMPLAINING OF SEVERE DRY EYE, IRRITATION AND PHOTOPHOBIA IN BOTH EYES POST TREATMENT. IT WAS REPORTED THAT THERE WAS NO LOSS OF BEST CORRECTED VISUAL ACUITY (BCVA). ON (B)(6) 2014, ABBOTT RECEIVED INFORMATION FROM THE ACCOUNT THAT DURING THE PATIENT'S LAST VISIT HE STATED THE SYMPTOMS HAVE NOT COMPLETELY RESOLVED HOWEVER, HE IS DOING MUCH BETTER AND BOTH THE DRYNESS AND THE PHOTOPHOBIA HAVE IMPROVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    349067 INTRALASE FS2 FEMTOSECOND LASER HNO ABBOTT MEDICAL OPTICS 20003D

    Patients

    Seq Age Sex Outcome Treatment
    1 47 YR Other