BEUDAMED
    FDA Adverse Event Summary report: N

    STERICYCLE SHARPS MANAGEMENT SERVICE

    MDR report key: 3042687 · Received April 3, 2013

    Report

    Report Number
    MW5029640
    Date Received
    April 3, 2013
    Date of Event
    February 12, 2013
    Report Date
    April 3, 2013
    Manufacturer
    STERICYCLE, INC
    Product Code
    MMK
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NM, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PT REMOVED SHARPS CONTAINER FROM A LOCKED SHARPS CONTAINER HOLDER THEN REMOVED ITEMS (SYRINGES AND PRESUMED EMPTY VIALS OF ATIVAN) FROM THE SHARPS CONTAINER BY TURNING IT UPSIDE DOWN. PLASTIC CONTAINER IS 45CM TALL, 26.5CM WIDE, 14CM DEEP. DIAMETER OF OPENING AT TOP OF CONTAINER IS 5.5 CM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    136796 STERICYCLE SHARPS MANAGEMENT SERVICE SHARPS CONTAINER, 45CM TALL, 26.5CM WIDE, 14CM DEEP MMK STERICYCLE, INC

    Patients

    Seq Age Sex Outcome Treatment
    1 35 YR Other