BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    KENDALL 1 QT N/S CONTAINER RED 100

    MDR report key: 714507 · Received May 12, 2006

    Report

    Report Number
    1424643-2006-00004
    Event Type
    Malfunction
    Date Received
    May 12, 2006
    Date of Event
    April 27, 2006
    Report Date
    May 9, 2006
    Manufacturer
    TYCO HEALTHCARE / KENDALL
    Product Code
    JKA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED TO TYCO HEALTHCARE /KENDALL ON 04/2006 THAT A CUSTOMER HAD A PROBLEM WITH A SHARPS CONTAINER. THE CUSTOMER STATES THAT SHE RECEIVED A CONTAMINATED NEEDLE STICK WHEN A NEEDLE WAS POKING THROUGH THE FRONT, RIGHT -SIDE BOTTOM CORNER OF THE CONTAINER.

    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 8900SA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN