BEUDAMED
    FDA Adverse Event Other Summary report: N

    IN-ROOM SHARPSTAR SHARPS DISPOSAL CONTAINER

    MDR report key: 92638 · Received May 20, 1997

    Report

    Report Number
    1419181-1997-00060
    Event Type
    Other
    Date Received
    May 20, 1997
    Date of Event
    February 21, 1997
    Report Date
    May 20, 1997
    Manufacturer
    SAGE PRODUCTS, INC.
    Product Code
    MMK
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    RN PUT NEEDLE/SYRINGE INTO LID/DOOR AND LIFTED LID/DOOR AND REPORTEDLY SOMEHOW THE NEEDLE/SYRINGE CAME OUT AND THE RN 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. 8508 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN