BEUDAMED
    FDA Adverse Event Other Summary report: N

    1219930AR IN-ROOM SHARPS DISPOSAL CONTAINER

    MDR report key: 197540 · Received November 13, 1998

    Report

    Report Number
    1419181-1998-00078
    Event Type
    Other
    Date Received
    November 13, 1998
    Date of Event
    September 1, 1998
    Report Date
    October 30, 1998
    Manufacturer
    SAGE PRODUCTS, INC.
    Product Code
    MMK
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ME, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    REPORTER DESCRIBED EVENT AS FOLLOWS: NURSE PLACED A NEEDLE/SYRINGE INTO THE LID/DOOR OF THE SHARPS CONTAINER. THE NURSE "FLIPPED" THE LID/DOOR INSTEAD OF LIFTING AND REPORTEDLY SOMEHOW RECEIVED A NEEDLESTICK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 1219930AR IN-ROOM SHARPS DISPOSAL CONTAINER 1996PS DISPOSAL CONTAINER MMK SAGE PRODUCTS, INC. 8508 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN