BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LATEX GLOVE

    MDR report key: 17869 · Received November 18, 1994

    Report

    Report Number
    MW1004087
    Event Type
    Injury
    Date Received
    November 18, 1994
    Date of Event
    March 24, 1994
    Report Date
    April 26, 1994
    Manufacturer
    UNKNOWN
    Product Code
    LYY
    Report Source
    Voluntary report
    Reporter Location
    IN, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    RPTR HAS HAD PROBLEMS FOR APPROX 1 YR WITH RUNNY NOSE AND SNEEZING WHILE WORKING AT THE HOSP. HER POSITION IS IV THERAPIST NURSE AND SAME DAY SURGERY NURSE. ALLERGY SYMPTOMS HAVE BECOME WORSE. RECENTLY, ON 4/24/94, SHE STARTED AN IV ON A PT AND WITHOUT WASHING HER HANDS HER RT EYE BECAME IRRITED. SHE BEGAN TO RUB HER EYES/ O,,EDOATE;U JER EUE BECA,E RED. SWP;;EM AMD VERU ORROTATED. SHE HAD TO SEEK MEDICAL TREATMENT. SHE WAS GIVEN A STEROID EYE OINTMENT WITHOUT HAVING HER EYE IRRIGATED WITH 500 CC NS WITH THE USE OF A MORGAN LENS. SHE HAS HAD HER EYES BECOME IRRITATED AT WORK BEFORE BUT IT WAS SHORT LIVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LATEX GLOVE LATEX GLOVE LYY UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 33 YR Other