BEUDAMED
    FDA Adverse Event Other Summary report: N

    DURASOFT 2 LITE EYES AQUA

    MDR report key: 242078 · Received September 24, 1999

    Report

    Report Number
    2648694-1999-00004
    Event Type
    Other
    Date Received
    September 24, 1999
    Date of Event
    August 25, 1999
    Report Date
    September 23, 1999
    Manufacturer
    WESLEY JESSEN INC.
    Product Code
    LPL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    PATIENT SUFFERED "CORNEAL BURNS" AFTER WEARING DURASOFT 2 LITE EYES AQUA CONTACT LENSES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DURASOFT 2 LITE EYES AQUA CONTACT LENS LPL WESLEY JESSEN INC. DURASOFT 2 LITE EYES AQUA 7960285002050034

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention