BEUDAMED
    FDA Adverse Event Other Summary report: N

    UNK

    MDR report key: 228259 · Received June 17, 1999

    Report

    Report Number
    2084395-1999-00111
    Event Type
    Other
    Date Received
    June 17, 1999
    Report Date
    June 17, 1999
    Manufacturer
    SAFESKIN CORP.
    Product Code
    LYY
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    ON MAY 21, 1999 SAFESKIN CORPORATION WAS SERVED WITH THE FOLLOWING LAWSUIT: PLAINTIFF'S CLAIM ALLEGES THE FOLLOWING: ON OR ABOUT NOVEMBER 21, 1997, PLAINTIFF SUFFERED A SEVERE ALLERGIC REACTION TO LATEX GLOVES. SHE WAS DIAGNOSED AS SUFFERING WITH SEVERE 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