BEUDAMED
    FDA Adverse Event Other Summary report: N

    IN-ROOM SHARPSTAR SHARPS DISPOSAL CONTAINER

    MDR report key: 112394 · Received August 5, 1997

    Report

    Report Number
    1419181-1997-00052
    Event Type
    Other
    Date Received
    August 5, 1997
    Date of Event
    September 8, 1996
    Report Date
    October 15, 1996
    Manufacturer
    SAGE PRODUCTS, INC.
    Product Code
    MMK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    REPORTER DESCRIBED EVENT AS FOLLOWS: HEALTHCARE WORKER PLACED NEEDLES/SYRINGE IN LID/DOOR "FLIPPED LID/DOOR" AND REPORTEDLY SOMEHOW NEEDLE/SYRINGE TUMBLED OUT AND HEALTHCARE WORKER RECEIVED A NEEDLESTICK.

    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. 8536 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN