BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SAGE

    MDR report key: 111252 · Received July 31, 1997

    Report

    Report Number
    MW1011842
    Event Type
    Malfunction
    Date Received
    July 31, 1997
    Date of Event
    July 10, 1997
    Report Date
    July 11, 1997
    Manufacturer
    SAGE PRODUCTS, INC.
    Product Code
    MMK
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IN, US
    Reporter Occupation
    BIOMEDICAL ENGINEER

    Narratives

    Description of Event or Problem · 1

    A PERSON WAS HANDLING A TRASH BAG, WHEN THEY WERE STUCK BY A NEEDLE THAT WAS PROTRUDING THROUGH THE SIDE OF A DISCARDED NEEDLE BOX, WHICH WAS IN THE TRASH BAG.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SAGE NEEDLE BOX MMK SAGE PRODUCTS, INC. R7042G NA

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other