BEUDAMED
    FDA Adverse Event Injury Summary report: N

    POWDERED LATEX GLOVE

    MDR report key: 35873 · Received August 23, 1996

    Report

    Report Number
    MW1009800
    Event Type
    Injury
    Date Received
    August 23, 1996
    Date of Event
    June 20, 1996
    Report Date
    August 22, 1996
    Manufacturer
    UNK
    Product Code
    LYY
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NJ, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    THE GLOVES SNAPPED UPON REMOVAL AND THE RPTR INHALED THE LATEX POWDER. SUBSEQUENTLY, THE RPTR DEVELOPED RESPIRATORY DISTRESS AND STRIDOR FOR WHICH SHE RECEIVED IV BENADRYL, SUB-Q EPINEPHRINE, O2 AND AN UNKNOWN NEBULIZER TREATMENT. RAST TEST WAS 35 AND RPTR WAS DIAGNOSED AS LATEX SENSITIVE BY TWO MDS.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR