BEUDAMED
    FDA Adverse Event Other Summary report: N

    1 QT N/S CONTAINDER RBD 100

    MDR report key: 485268 · Received September 25, 2003

    Report

    Report Number
    1424643-2003-00008
    Event Type
    Other
    Date Received
    September 25, 2003
    Report Date
    September 25, 2003
    Manufacturer
    TYCOHEALTHCARE/KENDALL
    Product Code
    MMK
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    PARAMEDIC

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED TO TYCOKENDALL THAT A CUSTOMER HAD A PROBLEM WITH A SHARPS CONTAINER. ACCORDING TO THE CUSTOMER A "NEEDLE PERFORATED SIDE OF CONTAINER AND STUCK A PARAMEDIC."

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 1 QT N/S CONTAINDER RBD 100 SHARPS CONTAINER MMK TYCOHEALTHCARE/KENDALL * UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 Other