BEUDAMED
    FDA Adverse Event Other Summary report: N

    KROGER DISINFECTING LENS CARE SOLUTON

    MDR report key: 2065559 · Received April 1, 2011

    Report

    Report Number
    2026940-2011-00002
    Event Type
    Other
    Date Received
    April 1, 2011
    Date of Event
    February 16, 2011
    Report Date
    March 31, 2011
    Manufacturer
    KC PHARMACEUTICALS, INC.
    Product Code
    LPN
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    AS DIAGNOSED BY URGENT CARE: ONE PATIENT EXPERIENCED CONJUNCTIVITIS AND SUPERFICIAL INJURY TO THE CORNEA AFTER USING MEDICAL DEVICE, KROGER DISINFECTING LENS CARE SOLUTION. PATIENT WAS PRESCRIBED TOBRAMYCIN SULFATE AND HYDROCODONE-ACETOMINOPHEN AS A RESULT

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KROGER DISINFECTING LENS CARE SOLUTON LPN KC PHARMACEUTICALS, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 Other