BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CURITY LATEX GLOVE

    MDR report key: 38982 · Received September 23, 1996

    Report

    Report Number
    MW1009962
    Event Type
    Injury
    Date Received
    September 23, 1996
    Date of Event
    April 1, 1992
    Report Date
    April 17, 1996
    Manufacturer
    KENDALL HEALTHCARE PRODUCTS CO.
    Product Code
    LYY
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    RPTR HAS BEEN HAVING REDDENED HANDS WITH USE OF LATEX GLOVES AT WORK. THIS HAS BEEN OCCURRING SINCE 1992. HAVE BEEN TO SEVERAL DOCTORS, ALLERGISTS, DERMATOLOGISTS ETC. RPTR'S HANDS HAVE BURNED SO BADLY SHE DOESN'T WANT TO USE GLOVES DURING PT CARE, ETC. RPTR WAS PUT OUT OF WORK FOR 2 DAYS UNTIL THE ENVIRONMENT COULD BE EVALUATED FOR LATEX CONTACTS. RPTR HAS HAD SEVERAL SINUS SURGERIES THAT SHE WAS TOLD COULD BE RELATED TO CONTACT WITH LATEX PRODUCTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CURITY LATEX GLOVE LATEX GLOVE LYY KENDALL HEALTHCARE PRODUCTS CO. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 34 YR Required Intervention| S