BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RENU WITH MOISTURELOC

    MDR report key: 699954 · Received April 13, 2006

    Report

    Report Number
    MW1038504
    Event Type
    Injury
    Date Received
    April 13, 2006
    Date of Event
    November 21, 2005
    Report Date
    April 11, 2006
    Manufacturer
    BAUSCH AND LOMB
    Product Code
    LPN
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    ID, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I WAS DIAGNOSED WITH FUNGAL KERATITIS. I WAS DIAGNOSED FOLLOWING A CORNEAL SCRAPING ON 11/21/2005. FORTUNATELY MY OPHTHALMOLOGIST DIAGNOSED IT QUICKLY SO I REC'D TREATMENT AND THE DAMAGE TO MY CORNEA IS OUTSIDE MY FIELD OF VISION. I AM A CONTACT LENSE WEARER AND I WAS USING RENU WITH MOISTURELOC AT THE TIME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RENU WITH MOISTURELOC MULTI-PURPOSE CONTACT LENSE SOLUTION. LPN BAUSCH AND LOMB * GK4112

    Patients

    Seq Age Sex Outcome Treatment
    1 37 YR Disability