BEUDAMED
    FDA Adverse Event Other Summary report: N

    UNK

    MDR report key: 225187 · Received May 26, 1999

    Report

    Report Number
    2084395-1999-00102
    Event Type
    Other
    Date Received
    May 26, 1999
    Report Date
    May 26, 1999
    Manufacturer
    SAFESKIN CORP.
    Product Code
    LYY
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    ON APRIL 30, 1999 SAFESKIN CORPORATION WAS SERVED WITH THE FOLLOWING LAWSUIT: PLAINTIFF'S CLAIM ALLEGES FOLLOWING: PLAINTIFF WORKED IN THE NEUROSURGICAL INTENSIVE CARE UNIT AND STOPPED WEARING LATEX GLOVES ON OR ABOUT APRIL 15, 1996, AFTER SHE DISCOVERED THAT WEARING LATEX GLOVES MIGHT BE CAUSING HER TO DEVELOP RESPIRATORY SYMPTOMS. PLAINTIFF WAS DIAGNOSED AS SUFFERING FROM LATEX ALLERGIES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNK LATEX GLOVE LYY SAFESKIN CORP. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other