BEUDAMED
    FDA Adverse Event Injury Summary report: N

    STICK-IT SHARPS CONTAINER

    MDR report key: 249465 · Received October 29, 1999

    Report

    Report Number
    MW4002630
    Event Type
    Injury
    Date Received
    October 29, 1999
    Date of Event
    October 22, 1999
    Report Date
    October 28, 1999
    Manufacturer
    EM INNOVATIONS, INC.
    Product Code
    MMK
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    NO INFORMATION

    Narratives

    Description of Event or Problem · 1

    NEEDLE STICK ON 10/22. REPORTED TO RPTR ON 10/28 AT 2:25 PM. MADE SURE NEEDLE AND CONTAINER WERE GUARDED AGAINST FURTHER PROBLEMS. INCIDENT STILL UNDER INVESTIGATION BY USER AND WILL SUBMIT AN ADDENDUM WHEN INVESTIGATION IS COMPLETE.INITIAL REPORT: WHILE DOING MORNING EQUIPMENT CHECKS FF/MEDIC WAS STUCK WITH A SHARP (16 GA ANGIO) STICKING THROUGH THE SIDE OF THE SHARPS BOX. IT WAS UNCLEAR HOW OR WHEN THE SHARP CAME THROUGH THE BOX. FF/MEDIC WAS SENT FOR STANDARD BLOOD TESTING PER DEPT POLICY. AN INJURY REPORT, WORKER'S COMP PAPERWORK AND NARRATIVE WERE FILLED OUT. THERE WERE PHOTOS TAKEN OF THE BOX ALSO.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STICK-IT SHARPS CONTAINER SHARPS CONTAINER MMK EM INNOVATIONS, INC. NI NI

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO