BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTURION

    MDR report key: 24641928 · Received March 19, 2026

    Report

    Report Number
    1824619-2026-00002
    Event Type
    Malfunction
    Date Received
    March 19, 2026
    Date of Event
    January 28, 2026
    Report Date
    March 19, 2026
    Manufacturer
    CENTURION MEDICAL PRODUCTS, LP
    Product Code
    JOK
    UDI-DI
    10653160008798
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    ACCORDING TO THE FACILITY, THE CUTTERS WOULD NOT CUT THROUGH A THIN WIRE BRONCHOSCOPY BRUSH WIRE. THE PT WAS HAVING A BRONCHOSCOPY AND BIOPSY OF A LUNG MASS. THE BRUSHING OF THE MASS WAS DONE AND THEN WHEN WE TRIED TO CUT THE BRUSH IN THE CYTOLYT. IT TOOK AT LEAST 20 TRIES TO CUT THE BRUSH OFF AND WHILE WE WERE OPENING AND CLOSING THE SCISSORS- WIRE CUTTERS THE SPECIMEN WAS FLINGING AND TOUCHING THE SIDES AND OUTSIDE OF THE CONTAINER. THIS WIRE CUTTER DID NOT EVEN CUT THE THIN WIRE. NO MEDICAL INTERVENTION, SERIOUS INJURY, OR FOLLOW-UP CARE HAS BEEN REPORTED. AT THIS TIME, NO INFORMATION HAS BEEN RECEIVED TO INDICATE THAT RECURRENCE OF THE COMPLAINT-SPECIFIC SEQUENCE OF EVENTS DETAILED BY THE CUSTOMER CONTACT MAY LIKELY CAUSE OR CONTRIBUTE TO A DEATH OR SERIOUS INJURY. NO ADVERSE EVENT REPORT WILL BE FILED AT THIS TIME. IF ADDITIONAL RELEVANT INFORMATION BECOMES AVAILABLE THIS INVESTIGATION WILL BE RE-OPENED AND RE-EVALUATED.

    Description of Event or Problem · 0

    ACCORDING TO THE FACILITY, THE CUTTERS WOULD NOT CUT THROUGH A THIN WIRE BRONCHOSCOPY BRUSH WIRE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    703871 CENTURION WIRE CUTTER, STERILE (WCS144) JOK CENTURION MEDICAL PRODUCTS, LP 10653160008798

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown