BEUDAMED
    FDA Adverse Event Other Summary report: N

    UNK

    MDR report key: 250834 · Received November 19, 1999

    Report

    Report Number
    2084395-1999-00144
    Event Type
    Other
    Date Received
    November 19, 1999
    Report Date
    November 19, 1999
    Manufacturer
    SAFESKIN CORPORATION
    Product Code
    LYY
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NH, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    ON OCTOBER 22, 1999, SAFESKIN CORPORATION WAS SERVED WITH THE FOLLOWING LAWSUIT: PLAINTIFFS CLAIM ALLEGES THE FOLLOWING: LATEX ALLERGY, IMMEDIATE-TYPE HYPERSENSITIVITY REACTION TO LATEX, ASTHMA.

    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