BEUDAMED
    FDA Adverse Event Other Summary report: N

    UNK

    MDR report key: 232399 · Received July 19, 1999

    Report

    Report Number
    2084395-1999-00119
    Event Type
    Other
    Date Received
    July 19, 1999
    Report Date
    July 19, 1999
    Manufacturer
    SAFESKIN CORPORATION
    Product Code
    LYY
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    ON JUNE 22, 1999 SAFESKIN CORPORATION WAS SERVED WITH THE FOLLOWING LAWSUIT; PLAINTIFF'S CLAIM ALLEGES THE FOLLOWING: TYPE I LATEX ALLERGY; ALLERGIC RHINITIS; DERMATITIS; WHEEZING; ANGIOEDEMA; URTICARIA.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other