BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    UNKNOWN DILATION PRODUCTS

    MDR report key: 25044832 · Received April 30, 2026

    Report

    Report Number
    1018233-2026-02773
    Event Type
    Malfunction
    Date Received
    April 30, 2026
    Date of Event
    April 23, 2026
    Report Date
    May 8, 2026
    Manufacturer
    C.R. BARD INC. (COVINGTON) -1018233
    Product Code
    FBW
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    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.

    Description of Event or Problem · 0

    CRITICAL CARE NURSES REPORTED IN AN ONLINE SURVEY STATE THAT NO THE PATIENT WAS NOT STONE FREE AT PROCEDURE COMPLETION. IN RELATION TO X-FORCE NEPHROSTOMY BALLOON DILATION CATHETER WITHOUT EAGLE INFLATION DEVICE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    396353 UNKNOWN DILATION PRODUCTS DILATION PRODUCT FBW C.R. BARD INC. (COVINGTON) -1018233 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other