BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BARD NASOGASTRIC SUMP TUBE

    MDR report key: 21839606 · Received April 15, 2025

    Report

    Report Number
    21839606
    Event Type
    Malfunction
    Date Received
    April 15, 2025
    Date of Event
    February 26, 2025
    Report Date
    April 9, 2025
    Manufacturer
    C. R. BARD, INC.
    Product Code
    BSS
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MO
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    AFTER PLACING AN OGT [OROGASTRIC TUBE] FOR GASTRIC DECOMPRESSION, THE OGT WAS VERIFIED WITH A KUB [KIDNEY, URETER, AND BLADDER X-RAY] AND THEN HOOKED UP TO SUCTION AND WHISTLING WAS NOTED, AND THE SUCTION WAS NOT WORKING. UPON INSPECTION OF THE TUBE, THE OPENING BETWEEN THE CLEAR PART OF THE TUBE AND THE PIGTAIL WAS TORN IN TWO PLACES, CAUSING THE AIR FROM THE SUCTION TO PULL THROUGH THE HOLE IN THE TORN TUBE RATHER THAN FROM THE PT'S (PATIENT'S) STOMACH. THE TUBE HAD TO BE REMOVED, REPLACED, AND RE-VERIFIED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    114329 BARD NASOGASTRIC SUMP TUBE TUBE, NASOGASTRIC BSS C. R. BARD, INC. 0042180 NGJV3240

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown