BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNK

    MDR report key: 317793 · Received February 20, 2001

    Report

    Report Number
    1520348-2001-00015
    Event Type
    Injury
    Date Received
    February 20, 2001
    Date of Event
    April 1, 2000
    Report Date
    February 2, 2001
    Manufacturer
    ANSELL
    Product Code
    LYY
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    THE LEGAL COMPLAINT STATES THAT THE INDIVIDUAL BECAME ALLERGIC TO LATEX AS A RESULT OF THE EXPOSURE TO AND WEARING OF LATEX MEDICAL GLOVES USED IN THE PERFORMANCE OF THEIR JOB DUTIES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    6731 UNK LATEX MEDICAL GLOVES LYY ANSELL UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 41 YR Disability