BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CUSTOM-MADE TREO ABDOMINAL STENT-GRAFT SYSTEM

    MDR report key: 20981845 · Received December 19, 2024

    Report

    Report Number
    2247858-2024-00332
    Event Type
    Injury
    Date Received
    December 19, 2024
    Date of Event
    October 2, 2024
    Report Date
    May 2, 2025
    Manufacturer
    BOLTON MEDICAL, INC.
    Product Code
    MIH
    PMA / PMN Number
    P190015
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NL
    Reporter Occupation
    OTHER
    Health Professional
    N

    Narratives

    Additional Manufacturer Narrative · 0

    THIS COMPLAINT WAS INVOLVED WITH FIVE DEVICES. DEVICE 1 IS BEING REPORTED UNDER MDR-2247858-2024-00332, DEVICE 2 IS BEING REPORTED UNDER MDR-2247858-2024-00338, DEVICE 3 IS BEING REPORTED UNDER MDR-2247858-2024-00339, DEVICE 4 IS BEING REPORTED UNDER MDR-2247858-2024-00340, AND DEVICE 5 IS BEING REPORTED UNDER MDR-2247858-2024-00341. BOLTON MEDICAL IS VOLUNTARILY REPORTING AN EVENT RELATED TO A TREO CUSTOM-MADE DEVICE. THE CUSTOM MADE TREO DEVICES ARE NOT MARKETED IN THE US, HOWEVER THEY ARE SIMILAR TO THE TREO ABDOMINAL STENT GRAFT DELIVERY SYSTEM APPROVED FOR SALE IN THE US (P190015). THE EVENT OCCURRED IN THE NETHERLANDS. BOLTON MEDICAL, INC. (D/B/A TERUMO AORTIC), HEREIN KNOWN AS THE "COMPANY", IS SUBMITTING THIS REPORT PURSUANT TO 21 CFR PART 803, HAS MADE REASONABLE EFFORTS TO OBTAIN COMPLETE INFORMATION, AND HAS PROVIDED AS MUCH AS IS AVAILABLE TO THE COMPANY AS OF THE SUBMISSION DATE OF THIS REPORT. THIS REPORT IS BASED ON INFORMATION OBTAINED BY THE COMPANY, WHICH MAY NOT HAVE BEEN ABLE TO FULLY INVESTIGATE OR VERIFY PRIOR TO THE DATE THE REPORT WAS REQUIRED BY THE REGULATIONS. ANY REQUIRED FIELDS THAT ARE UNPOPULATED ARE BLANK BECAUSE THE INFORMATION IS CURRENTLY UNKNOWN, UNAVAILABLE, OR NOT APPLICABLE. THIS REPORT DOES NOT CONSTITUTE AN ADMISSION OR A CONCLUSION BY ANYONE THAT THE DEVICE CAUSED OR CONTRIBUTED TO THE EVENT DESCRIBED IN THE REPORT. IN PARTICULAR, THIS REPORT DOES NOT CONSTITUTE A LEGAL ADMISSION BY ANYONE THAT THE PRODUCT DESCRIBED IN THIS REPORT HAS ANY DEFECTS OR HAS MALFUNCTIONED, AS DEFINED FROM A LEGAL STANDPOINT. THESE WORDS ARE INCLUDED IN THE REPORT AND ARE FIXED ITEMS FOR SELECTION CREATED BY THE CERTAIN REGULATIONS, TO CATEGORIZE THE TYPE OF EVENT SOLELY FOR THE PURPOSE OF REPORTING PURSUANT TO PART 803. THIS STATEMENT SHOULD BE INCLUDED WITH ANY INFORMATION OR REPORT DISCLOSED TO THE PUBLIC UNDER THE FREEDOM OF INFORMATION ACT.

    Additional Manufacturer Narrative · 0

    THIS COMPLAINT WAS INVOLVED WITH FIVE DEVICES. DEVICE 1 IS BEING REPORTED UNDER MDR-2247858-2024-00332, DEVICE 2 IS BEING REPORTED UNDER MDR-2247858-2024-00338, DEVICE 3 IS BEING REPORTED UNDER MDR-2247858-2024-00339, DEVICE 4 IS BEING REPORTED UNDER MDR-2247858-2024-00340, AND DEVICE 5 IS BEING REPORTED UNDER MDR-2247858-2024-00341. BOLTON MEDICAL IS VOLUNTARILY REPORTING AN EVENT RELATED TO A TREO CUSTOM-MADE DEVICE. THE CUSTOM-MADE TREO DEVICES ARE NOT MARKETED IN THE US; HOWEVER, THEY ARE SIMILAR TO THE TREO ABDOMINAL STENT GRAFT DELIVERY SYSTEM APPROVED FOR SALE IN THE US ((B)(6)). THE EVENT OCCURRED IN THE NETHERLANDS. BOLTON MEDICAL, INC. (D/B/A TERUMO AORTIC), HEREIN KNOWN AS THE "COMPANY", IS SUBMITTING THIS REPORT PURSUANT TO 21 CFR PART 803, HAS MADE REASONABLE EFFORTS TO OBTAIN COMPLETE INFORMATION, AND HAS PROVIDED AS MUCH AS IS AVAILABLE TO THE COMPANY AS OF THE SUBMISSION DATE OF THIS REPORT. THIS REPORT IS BASED ON INFORMATION OBTAINED BY THE COMPANY, WHICH MAY NOT HAVE BEEN ABLE TO FULLY INVESTIGATE OR VERIFY PRIOR TO THE DATE THE REPORT WAS REQUIRED BY THE REGULATIONS. ANY REQUIRED FIELDS THAT ARE UNPOPULATED ARE BLANK BECAUSE THE INFORMATION IS CURRENTLY UNKNOWN, UNAVAILABLE, OR NOT APPLICABLE. THIS REPORT DOES NOT CONSTITUTE AN ADMISSION OR A CONCLUSION BY ANYONE THAT THE DEVICE CAUSED OR CONTRIBUTED TO THE EVENT DESCRIBED IN THE REPORT. IN PARTICULAR, THIS REPORT DOES NOT CONSTITUTE A LEGAL ADMISSION BY ANYONE THAT THE PRODUCT DESCRIBED IN THIS REPORT HAS ANY DEFECTS OR HAS MALFUNCTIONED, AS DEFINED FROM A LEGAL STANDPOINT. THESE WORDS ARE INCLUDED IN THE REPORT AND ARE FIXED ITEMS FOR SELECTION CREATED BY THE CERTAIN REGULATIONS, TO CATEGORIZE THE TYPE OF EVENT SOLELY FOR THE PURPOSE OF REPORTING PURSUANT TO PART 803. THIS STATEMENT SHOULD BE INCLUDED WITH ANY INFORMATION OR REPORT DISCLOSED TO THE PUBLIC UNDER THE FREEDOM OF INFORMATION ACT.

    Description of Event or Problem · 0

    "PATIENT (B)(6) A 77-YEAR-OLD MALE WITH AAA (ABDOMINAL AORTIC ANEURYSM) EXPERIENCED AN EVENT "TYPE 1B ENDOLEAK BOTH SIDES' ON THE (B)(6) 2024. THIS WAS AN ANTICIPATED EVENT, IT IS NOT RELATED TO PRE-EXISTING CONDITIONS AND NOT RELATED TO THE PROCEDURE. IT IS UNDETERMINED IF IT WAS RELATED TO THE DEVICE. THE ADVERSE EVENT IS CURRENTLY ONGOING. DURING THE PROCEDURE THE METHOD OF ACCESS WAS GAINED VIA THE RIGHT AND LEFT COMMON FEMORAL. DURING THE PROCEDURE ANTICOAGULATION, ANTIPLATELET, AND ANTIBIOTIC TREATMENTS WERE ADMINISTERED." PATIENT OUTCOME: "ONGOING."

    Description of Event or Problem · 0

    "PATIENT (B)(6) A 77-YEAR-OLD MALE WITH AAA (ABDOMINAL AORTIC ANEURYSM) EXPERIENCED AN EVENT "TYPE 1B ENDOLEAK BOTH SIDES' ON THE (B)(6)2024. THIS WAS AN ANTICIPATED EVENT, IT IS NOT RELATED TO PRE-EXISTING CONDITIONS AND NOT RELATED TO THE PROCEDURE. IT IS UNDETERMINED IF IT WAS RELATED TO THE DEVICE. THE ADVERSE EVENT IS CURRENTLY ONGOING. DURING THE PROCEDURE THE METHOD OF ACCESS WAS GAINED VIA THE RIGHT AND LEFT COMMON FEMORAL. DURING THE PROCEDURE ANTICOAGULATION, ANTIPLATELET, AND ANTIBIOTIC TREATMENTS WERE ADMINISTERED." PATIENT OUTCOME: "ONGOING".

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2280432 CUSTOM-MADE TREO ABDOMINAL STENT-GRAFT SYSTEM STENT, ENDOVASCULAR GRAFT, AORTIC MIH BOLTON MEDICAL, INC. 2306190141

    Patients

    Seq Age Sex Outcome Treatment
    1 77 YR Male Other