BEUDAMED
    FDA Adverse Event Other Summary report: N

    MICRO-TOUCH LATEX MEDICAL GLOVES

    MDR report key: 259975 · Received January 26, 2000

    Report

    Report Number
    1618732-2000-00014
    Event Type
    Other
    Date Received
    January 26, 2000
    Report Date
    January 21, 2000
    Manufacturer
    JOHNSON & JOHNSON MEDICAL, MFG. SDN.BHD
    Product Code
    LYX
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    PLAINTIFF WAS EMPLOYED AS A REGISTERED NURSE WHO WORE AND WAS EXPOSED TO LATEX GLOVES MADE BY VARIOUS MANUFACTURERS. PLAINTIFF ALLEGES DEVELOPING A LATEX ALLERGY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MICRO-TOUCH LATEX MEDICAL GLOVES GLOVES, MEDICAL, LATEX LYX JOHNSON & JOHNSON MEDICAL, MFG. SDN.BHD NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other