BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SHARPS CONTAINER

    MDR report key: 33093 · Received May 7, 1996

    Report

    Report Number
    33093
    Event Type
    Malfunction
    Date Received
    May 7, 1996
    Date of Event
    April 24, 1996
    Report Date
    May 1, 1996
    Manufacturer
    SAGE PRODUCTS, INC.
    Product Code
    MMK
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CT, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    SUPERVISOR TRANSPORTING SHARPS CONTAINER FOR DISPOSAL IN BIOHAZARD BOX. NEEDLE PROTRUDING THROUGH SHARPS CONTAINER CAUSED NEEDLE STICK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SHARPS CONTAINER SHARPS CONTAINER MMK SAGE PRODUCTS, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 32 YR