BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CYTOCORE

    MDR report key: 24757152 · Received April 1, 2026

    Report

    Report Number
    MW5186238
    Event Type
    Injury
    Date Received
    April 1, 2026
    Date of Event
    March 23, 2026
    Report Date
    March 27, 2026
    Manufacturer
    PRAXIS MEDICAL LLC
    Product Code
    KNW
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    PATIENT UNDERWENT ULTRASOUND GUIDED THYROID BIOPSY, 25G NEEDLE BROKE OFF AND STUCK IN PATIENT'S THYROID BED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    811625 CYTOCORE INSTRUMENT, BIOPSY KNW PRAXIS MEDICAL LLC C0025 2507022

    Patients

    Seq Age Sex Outcome Treatment
    1 Male Hospitalization