BEUDAMED
    FDA Adverse Event Other Summary report: N

    LATEX EXAM GLOVES

    MDR report key: 362813 · Received November 29, 2001

    Report

    Report Number
    1423507-2001-00279
    Event Type
    Other
    Date Received
    November 29, 2001
    Date of Event
    July 31, 2000
    Report Date
    November 29, 2001
    Manufacturer
    ALLEGIANCE HEALTHCARE CORPORATION
    Product Code
    LYY
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NV, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    PLAINTIFF ALLEGES THAT WHILE WORKING AS A NURSE, PLAINTIFF WAS EXPOSED TO LATEX GLOVES, AND DEVDELOPED A TYPE 1 LATEX HYPERSENSITIVITY. PLAINTIFF ALLEGES THAT PLAINTIFF WAS DIAGNOSED IN 2000, WITH TYPE 1 LATEX HYPERSENSITIVITY. PLAINTIFF ALSO ALLEGES THAT PLAINTIFF HAS EXPERIENCED OR IS AT RISK OF EXPERIENCING SKIN RASHES, HIVES, SWELLING, ASTHMA, RESPIRATORY PROBLEMS SUCH AS DIFFICULTY BREATHING, WHEEZING, AND COUGHING, ANAPHYLACTIC SHOCK, AND DEATH. PLAINTIFF FURTHER ALLEGES DAMAGES SUFFERED, SUSTAINED, AND INCURRED, AND WILL CONTINUE IN THE FUTURE TO SUFFER, SUSTAIN AND INCUR, PHYSICAL PAIN AND SUFFERING, MENTAL ANGUISH, REASONABLE AND NECESSARY MEDICAL EXPENSES, PHYSICAL DISABILITY, PHYSICAL DISFIGUREMENT, AND LOSS OF EARNINGS AND/OR EARNING CAPACITY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    53867 LATEX EXAM GLOVES LATEX EXAM GLOVES LYY ALLEGIANCE HEALTHCARE CORPORATION UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other