BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DYNAREX SHARPS CONTAINER

    MDR report key: 5746357 · Received June 23, 2016

    Report

    Report Number
    2431014-2016-00001
    Event Type
    Malfunction
    Date Received
    June 23, 2016
    Date of Event
    March 14, 2016
    Report Date
    June 10, 2016
    Manufacturer
    DYNAREX CORPORATION
    Product Code
    MMK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    A NURSE WAS STUCK WITH A NEEDLE PROTRUDING THROUGH A SHARPS CONTAINER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    400406 DYNAREX SHARPS CONTAINER CONTAINER, SHARPS MMK DYNAREX CORPORATION 4624 31084

    Patients

    Seq Age Sex Outcome Treatment
    1 Other