BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    UNKNOWN NASOGASTRIC TUBE

    MDR report key: 24596013 · Received March 13, 2026

    Report

    Report Number
    1018233-2026-01732
    Event Type
    Malfunction
    Date Received
    March 13, 2026
    Date of Event
    March 10, 2026
    Report Date
    April 21, 2026
    Manufacturer
    C.R. BARD INC. (COVINGTON) -1018233
    Product Code
    BSS
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    PHYSICIAN
    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. THE REPORTED PRODUCT NUMBER IS UNKNOWN. THE UDI NUMBER FOR THIS PRODUCT IS NOT AVAILABLE. H11: SECTION 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.

    Additional Manufacturer Narrative · 0

    THE REPORTED EVENT WAS INCONCLUSIVE BECAUSE THIS INVESTIGATION DID NOT RESULT IN ANY ADDITIONAL FINDINGS AND NO SAMPLE WAS AVAILABLE FOR EVALUATION. THE PRODUCT CATALOG NUMBER AND THE LOT NUMBER FOR THIS DEVICE ARE UNKNOWN. THEREFORE, BD IS UNABLE TO DETERMINE THE ASSOCIATED LABELING TO REVIEW. A DHR COULD NOT BE PERFORMED SINCE NO LOT NUMBER WAS PROVIDED. THE REPORTED PRODUCT NUMBER IS UNKNOWN. THE UDI NUMBER FOR THIS PRODUCT IS NOT AVAILABLE. H11: SECTION 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 THE CUSTOMER HAD WANTED TO KNOW WHETHER BD MADE ANY ACCESSORIES FOR USE WITH THE BLAKEMORE TUBE. THE CUSTOMER HAD BEEN WATCHING A SETUP ON YOUTUBE AND HAD NOT HAD MUCH LUCK LOCATING THE ACCESSORY USED IN THE VIDEO. THEY FELT THAT USING A LOPEZ VALVE HAD BEEN DIFFICULT WITH THIS DEVICE, ESPECIALLY SINCE THE INSERTION HAD BEEN VERY BLOODY, MAKING IT HARD TO GRASP THE DEVICES.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE CUSTOMER HAD WANTED TO KNOW WHETHER BD MADE ANY ACCESSORIES FOR USE WITH THE BLAKEMORE TUBE. THE CUSTOMER HAD BEEN WATCHING A SETUP ON YOUTUBE AND HAD NOT HAD MUCH LUCK LOCATING THE ACCESSORY USED IN THE VIDEO. THEY FELT THAT USING A LOPEZ VALVE HAD BEEN DIFFICULT WITH THIS DEVICE, ESPECIALLY SINCE THE INSERTION HAD BEEN VERY BLOODY, MAKING IT HARD TO GRASP THE DEVICES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    31518 UNKNOWN NASOGASTRIC TUBE NASOGASTRIC TUBE BSS C.R. BARD INC. (COVINGTON) -1018233 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1