BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BARD® NASOGASTRIC SUMP TUBE

    MDR report key: 24879367 · Received April 14, 2026

    Report

    Report Number
    1018233-2026-02448
    Event Type
    Malfunction
    Date Received
    April 14, 2026
    Date of Event
    April 8, 2026
    Report Date
    May 14, 2026
    Manufacturer
    C.R. BARD INC. (COVINGTON) -1018233
    Product Code
    BSS
    UDI-DI
    00801741052255
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VT, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    THE INVESTIGATION IS STILL IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETE, A SUPPLEMENTAL REPORT WILL BE FILED. UDI FORMAT UPDATED WITH AVAILABLE PRODUCT INFORMATION PER GUDID. H11: SECTIONS A THROUGH F - THE INFORMATION PROVIDED BY BD REPRESENTS ALL THE KNOWN INFORMATION AT THIS TIME. DESPITE GOOD FAITH EFFORTS TO OBTAIN ADDITIONAL INFORMATION, THE COMPLAINANT / REPORTER WAS UNABLE OR UNWILLING TO PROVIDE ANY FURTHER PATIENT, PRODUCT, OR PROCEDURAL DETAILS TO BD.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT CUSTOMER HAD THIS BARD NASOGASTRIC TUBING 0042140 COME APART WHILE BEING USED IN A PATIENT. THE DEPARTMENT STAFF STATED THAT THE BLUE TUBING SHOULD NOT SEPARATE FROM THE CLEAR COMPONENT PART, BUT IT DID.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    254030 BARD® NASOGASTRIC SUMP TUBE NASOGASTRIC TUBE BSS C.R. BARD INC. (COVINGTON) -1018233 UNK 00801741052255

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other