BEUDAMED
    FDA Adverse Event Summary report: N

    KENDALL 1 QT N/S CONTAINER RED 100

    MDR report key: 637410 · Received September 26, 2005

    Report

    Report Number
    1424643-2005-00009
    Date Received
    September 26, 2005
    Report Date
    September 22, 2005
    Manufacturer
    TYCO HEALTHCARE/ KENDALL
    Product Code
    JKA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED TO TYCO HEALTHCARE/KENDALL IN 2005 THAT A CUSTOMER HAD A PROBLEM WITH A SHARP CONTAINER. ACCORDING TO THE CUSTOMER A NURSE RECEIVED A CONTAMINATED NEEDLE STICK. THE NEEDLE PUNCTURED THE CONTAINER AND STUCK THE NURSE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KENDALL 1 QT N/S CONTAINER RED 100 SHARPS CONTAINER JKA TYCO HEALTHCARE/ KENDALL UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other