BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNK

    MDR report key: 319831 · Received March 9, 2001

    Report

    Report Number
    1520348-2001-00025
    Event Type
    Injury
    Date Received
    March 9, 2001
    Date of Event
    October 1, 1997
    Report Date
    March 9, 2001
    Manufacturer
    ANSELL
    Product Code
    LYX
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, 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 "HIB" DUTIES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    10207 UNK LATEX MEDICAL GLOVES LYX ANSELL UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Disability