BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MEDLINE BIOHAZARD CONTAINER 5.4 QT

    MDR report key: 16854059 · Received May 1, 2023

    Report

    Report Number
    MW5117193
    Event Type
    Malfunction
    Date Received
    May 1, 2023
    Date of Event
    April 27, 2023
    Report Date
    April 27, 2023
    Manufacturer
    MEDLINE INDUSTRIES, LP-NORTHFIELD
    Product Code
    NNK
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IN, US
    Reporter Occupation
    RISK MANAGER
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    CONTAINERS PREVENT SHARPS PRODUCTS FROM FULLY FALLING INTO THE CONTAINER. THIS LEADS TO SHARPS DEVICES STICKING OUT CREATING A POTENTIAL NEEDLESTICK HAZARD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1740068 MEDLINE BIOHAZARD CONTAINER 5.4 QT CONTAINER, SPECIMEN MAILER AND STORAGE, NON-STERILE NNK MEDLINE INDUSTRIES, LP-NORTHFIELD MD5705253

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown