BEUDAMED
    FDA Adverse Event Other Summary report: N

    MICRO-TOUCH LATEX MEDICAL GLOVES

    MDR report key: 167030 · Received May 12, 1998

    Report

    Report Number
    1618732-1998-00116
    Event Type
    Other
    Date Received
    May 12, 1998
    Report Date
    April 15, 1998
    Manufacturer
    JOHNSON & JOHNSON MEDICAL, MFG, SDN.BHD
    Product Code
    LYX
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    A REGISTERED NURSE REPORTED THAT SHE DEVELOPED AN ALLERGY TO LATEX. SHE STATES THAT SHE WORE LATEX GLOVES MADE BY VARIOUS GLOVE MFRS.

    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 NA Other