BEUDAMED
    FDA Adverse Event Injury Summary report: N

    COMPLETE MOISTURE PLUS 12 FL. OZ - 355ML STERILE

    MDR report key: 859680 · Received May 30, 2007

    Report

    Report Number
    MW5002215
    Event Type
    Injury
    Date Received
    May 30, 2007
    Date of Event
    May 29, 2007
    Report Date
    May 30, 2007
    Manufacturer
    ADVANCED MEDICAL OPTICS
    Product Code
    LPN
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    RI, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    I PURCHASED ADVANCED MEDICAL OPTICS COMPLETE MOISTUREPLUS CONTACT LENS SOLUTION THAT WAS PURCHASED ON MONDAY, 05/28/07 AT MY LOCAL TARGET STORE. I USED IT FOR THE FIRST TIME THE NEXT DAY. WITH IN HOURS, MY EYES BECAME VERY RED AND IRRITATED; IT FELT LIKE SOMETHING WAS IN MY EYES. MY EYES BECAME VERY TEARFUL AND LOOKED LIKE LITTLE RED TOMATOES. I IN TURN TOOK MY LENSES OUT AND PUT MY GLASSES ON. THE NEXT DAY, MY EYES WERE CLEAR, SO I PUT MY LENSES AND AGAIN USED ADVANCED MEDICAL OPTICS COMPLETE MOISTUREPLUS CONTACT LENS SOLUTION. AGAIN, MY EYES BECAME VERY RED AND IRRITATED, FEELING LIKE SOMETHING WAS IN MY EYE, AND TEARY. IT WAS THEN THAT A COWORKER STATED THAT A CONTACT LENS SOLUTION HAD BEEN RECALLED, SO I CHECKED THE FDA WEBSITE AND SAW THAT MY LENS SOLUTION WAS RECALLED; SO I AM REPORTING MY REACTION TO THIS SOLUTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 COMPLETE MOISTURE PLUS 12 FL. OZ - 355ML STERILE NONE LPN ADVANCED MEDICAL OPTICS AC00730

    Patients

    Seq Age Sex Outcome Treatment
    1 YR