BEUDAMED
    FDA Adverse Event Other Summary report: N

    IN-ROOM SHARPS DISPOSAL CONTAINER

    MDR report key: 39809 · Received September 4, 1996

    Report

    Report Number
    1419181-1996-00045
    Event Type
    Other
    Date Received
    September 4, 1996
    Date of Event
    April 24, 1996
    Report Date
    September 4, 1996
    Manufacturer
    SAGE PRODUCTS, INC.
    Product Code
    MMK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NM, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    AFTER ADMINISTERING A S.Q. INJECTION, PUT NEEDLE INTO THE DISPOSAL AND IT PRICKED THE INDEX FINGER ON MY RIGHT HAND. REPORTEDLY "FLIPPED" IN TRAY OF THE SHARPS BOX.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IN-ROOM SHARPS DISPOSAL CONTAINER SHARPS DISPOSAL CONTAINER MMK SAGE PRODUCTS, INC. 8508-MW UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO