BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CHANNEL DRAIN

    MDR report key: 24749089 · Received March 31, 2026

    Report

    Report Number
    1018233-2026-02124
    Event Type
    Malfunction
    Date Received
    March 31, 2026
    Date of Event
    March 25, 2026
    Report Date
    May 5, 2026
    Manufacturer
    C.R. BARD INC. (COVINGTON) -1018233
    Product Code
    GBX
    UDI-DI
    00801741049897
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, 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. UDI FORMAT UPDATED WITH AVAILABLE PRODUCT INFORMATION PER GUDID. 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 RECENTLY CONVERTED OUR BLAKE DRAINS TO THE BD 072227 DRAINS. CUSTOMER WAS RECEIVING SOME COMPLAINTS ON THE BD DRAINS, PRIMARILY ON THE SIZE OF THE TROCAR COMPARED TO THE BLAKE DRAINS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    609807 CHANNEL DRAIN WOUND DRAIN GBX C.R. BARD INC. (COVINGTON) -1018233 UNK 00801741049897

    Patients

    Seq Age Sex Outcome Treatment
    1