BEUDAMED
    FDA Adverse Event Other Summary report: N

    1QT. HMCARE SHRPS DISP.CONT.20

    MDR report key: 2974247 · Received February 14, 2013

    Report

    Report Number
    1424643-2013-00001
    Event Type
    Other
    Date Received
    February 14, 2013
    Report Date
    January 21, 2013
    Manufacturer
    COVIDIEN
    Product Code
    MMK
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    SUBMIT DATE: (B)(4) 2013. AN INVESTIGATION IS CURRENTLY UNDERWAY, UPON COMPLETION THE RESULTS WILL BE FORWARDED.

    Description of Event or Problem · 1

    IT WAS REPORTED TO COVIDIEN ON (B)(6) 2013 THAT A CUSTOMER HAD AN ISSUE WITH A SHARPS DISPOSAL CONTAINER. THE CUSTOMER REPORTS A NEEDLE PENETRATED THE SHARPS CONTAINER AND STUCK THE NURSE. THE NURSE FOLLOWED NORMAL HOSPITAL PROCEDURE FOR A NEEDLE STICK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    66187 1QT. HMCARE SHRPS DISP.CONT.20 SHARPS DISPOSAL CONTAINER MMK COVIDIEN 8303SA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Other