BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    IN-ROOM SHARPSTAR SHARPS DISPOSAL CONTAINER

    MDR report key: 43124 · Received September 6, 1996

    Report

    Report Number
    1419181-1996-00048
    Event Type
    Malfunction
    Date Received
    September 6, 1996
    Date of Event
    January 11, 1996
    Report Date
    September 6, 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

    EMPLOYEE ALLEGES: DISCARDING OF USED NEEDLES IN SHARPS; LID JAMMED CAUSING NEEDLESTICK TO LEFT THUMB.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN