BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    8702 SHARP: 1 QT. RED

    MDR report key: 2954167 · Received February 4, 2013

    Report

    Report Number
    MW5028904
    Event Type
    Malfunction
    Date Received
    February 4, 2013
    Date of Event
    January 28, 2013
    Report Date
    February 4, 2013
    Manufacturer
    MEDICAL ACTION INDUSTRIES
    Product Code
    MMK
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    NURSE FINGER STUCK BY USED NEEDLE THAT HAD PENETRATED THROUGH SHARPS CONTAINER. SECOND EVENT OF SAME NATURE. DATES OF USE: (B)(6) 2012 - (B)(6) 2013. EVENT ABATED AFTER USE STOPPED OR DOSE REDUCED? YES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    45764 8702 SHARP: 1 QT. RED SHARPS CONTAINER MMK MEDICAL ACTION INDUSTRIES 150118

    Patients

    Seq Age Sex Outcome Treatment
    1 30 YR