BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CHANNEL DRAIN

    MDR report key: 24475628 · Received February 27, 2026

    Report

    Report Number
    1018233-2026-01379
    Event Type
    Malfunction
    Date Received
    February 27, 2026
    Date of Event
    February 23, 2026
    Report Date
    May 12, 2026
    Manufacturer
    C.R. BARD INC. (COVINGTON) -1018233
    Product Code
    GBX
    UDI-DI
    00801741049873
    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 BY THE CUSTOMER THAT THEY HAD REQUESTED A SAMPLE OF (B)(6). THE CUSTOMER STATED THAT THEY HAD A DOCTOR WHO USED PRODUCT 072227 AND HAD NOT LIKED THE TROCAR ATTACHED. THE DOCTOR WAS CURRENTLY USING 072227 WHICH WAS A DRAIN WITH A TROCAR. THEY WERE STATING THE TROCAR BENDS AND HAS ASKED TO FIND THEM SOMETHING ELSE TO USE. THE ONE SENT WAS OFF CONTRACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    71318 CHANNEL DRAIN WOUND DRAIN GBX C.R. BARD INC. (COVINGTON) -1018233 UNK 00801741049873

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other