BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    MEDLINE

    MDR report key: 16351088 · Received February 10, 2023

    Report

    Report Number
    16351088
    Event Type
    No answer provided
    Date Received
    February 10, 2023
    Date of Event
    January 12, 2023
    Report Date
    January 13, 2023
    Manufacturer
    MEDLINE INDUSTRIES, INC.
    Product Code
    LRP
    UDI-DI
    10653160349914
    Report Source
    User Facility report
    Reporter Location
    RI
    Reporter Occupation
    RISK MANAGER
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    A CRACKED SPECIMEN VIAL FOUND IN ULTRASOUND BIOPSY KIT. VIAL REMOVED, NO HARM OR DELAY TO PATIENT CARE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    43283 MEDLINE TRAY, SURGICAL LRP MEDLINE INDUSTRIES, INC. DYNDH1699 2022092790 10653160349914

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown