BEUDAMED
    FDA Adverse Event Other Summary report: N

    IN-ROOM SHARPS DISPOSAL CONTAINER

    MDR report key: 39805 · Received September 4, 1996

    Report

    Report Number
    1419181-1996-00044
    Event Type
    Other
    Date Received
    September 4, 1996
    Date of Event
    June 10, 1996
    Report Date
    September 3, 1996
    Manufacturer
    SAGE PRODUCTS, INC.
    Product Code
    MMK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OR, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    A PHLEBOTOMIST WAS GOING TO DISPOSE OF A NEEDLE/SYRINGE; AS SHE TRIED TO OPEN THE DOOR, REPORTEDLY A NEEDLE/SYRINGE CAME OUT AND SOMEHOW SHE RECEIVED A NEEDLESTICK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IN-ROOM SHARPS DISPOSAL CONTAINER SHARPS DISPOSAL CONTAINER MMK SAGE PRODUCTS, INC. 8513-1 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO