BEUDAMED
    FDA Adverse Event Other Summary report: N

    UNK

    MDR report key: 248368 · Received November 4, 1999

    Report

    Report Number
    2084395-1999-00142
    Event Type
    Other
    Date Received
    November 4, 1999
    Report Date
    November 4, 1999
    Manufacturer
    SAFESKIN CORP.
    Product Code
    LYY
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    ON OCTOBER 14, 1999, SAFESKIN CORP WAS SERVED WITH THE FOLLOWING LAWSUIT: PLAINTIFF'S CLAIM ALLEGES THE FOLLOWING: RESPIRATORY PROBLEMS, ANAPHYLACTIC REACTIONS, TYPE-1 LATEX ALLERGY.

    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