BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CLEARPRO¿ TRACH T-PIECE CLOSED SUCTION CATHETER, 14 FRENCH

    MDR report key: 25061037 · Received May 1, 2026

    Report

    Report Number
    1417592-2026-00787
    Event Type
    Malfunction
    Date Received
    May 1, 2026
    Date of Event
    March 31, 2026
    Report Date
    May 28, 2026
    Manufacturer
    MEDLINE INDUSTRIES, LP
    Product Code
    OFR
    UDI-DI
    10888277703469
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NE, US
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    PER REPORT, " THE SUCTION CATHETER CAME A PART WHILE BEING ATTACHED TO THE PATIENT FOR LESS THAN 12 HOURS." THERE WERE NO REPORTS OF DEATH, SERIOUS INJURY, MEDICAL INTERVENTION, OR FOLLOW UP CARE. IT HAS BEEN DETERMINED THAT THE REPORTED EVENT COULD CAUSE OR CONTRIBUTE TO SERIOUS INJURY IF IT WERE TO OCCUR AGAIN. IN AN ABUNDANCE OF CAUTION, THIS MEDWATCH IS BEING FILED. IF ANY FURTHER RELEVANT INFORMATION IS IDENTIFIED OR OBTAINED, A SUPPLEMENTAL MEDWATCH WILL BE SUBMITTED.

    Description of Event or Problem · 0

    PER REPORT, " THE SUCTION CATHETER CAME A PART WHILE BEING ATTACHED TO THE PATIENT FOR LESS THAN 12 HOURS."

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    482090 CLEARPRO¿ TRACH T-PIECE CLOSED SUCTION CATHETER, 14 FRENCH CLEARPRO,CLOSED SXN,14FR,T-PC,ETT OFR MEDLINE INDUSTRIES, LP 10888277703469

    Patients

    Seq Age Sex Outcome Treatment
    1