BEUDAMED
    FDA Adverse Event Other Summary report: N

    UNK

    MDR report key: 210017 · Received February 12, 1999

    Report

    Report Number
    2084395-1999-00005
    Event Type
    Other
    Date Received
    February 12, 1999
    Report Date
    February 12, 1999
    Manufacturer
    SAFESKIN CORP.
    Product Code
    LYY
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OR, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    ON 1/28/99, SAFESKIN CORP WAS SERVED WITH THE FOLLOWING LAWSUIT: PLAINTIFF'S CLAIM ALLEGES THE FOLLOWING: PLAINTIFF SUFFERS FROM TYPE I LATEX ALLERGY SYMPTOMS INCLUDING BUT NOT LIMITED TO URTICARIA, WHEEZING, SWELLING, DERMATITIS, IRRITATED EYES, RUNNY NOSE, DIFFICULTY BREATHING AND RISK OF ANAPHYLACTIC SHOCK.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other