BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RELAY PRO NBS THORACIC STENT-GRAFT SYSTEM

    MDR report key: 21242933 · Received January 27, 2025

    Report

    Report Number
    2247858-2025-00021
    Event Type
    Injury
    Date Received
    January 27, 2025
    Date of Event
    August 17, 2024
    Report Date
    October 23, 2025
    Manufacturer
    BOLTON MEDICAL, INC.
    Product Code
    MIH
    UDI-DI
    00843576150614
    PMA / PMN Number
    P200045
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    OTHER
    Health Professional
    N

    Narratives

    Additional Manufacturer Narrative · 0

    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

    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

    "IS THIS EVENT RELATED TO DEVICE FAILURE / DEFICIENCY? POSSIBLY IS THIS EVENT RELATED TO THE PROCEDURE? NO IS THIS EVENT RELATED TO A PRE-EXISTING CONDITION? NO WAS SURGICAL INTERVENTION REQUIRED. ADMITTED TO OUTSIDE HOSPITAL ON (B)(6) 2024 WITH LEFT SIDED HEMIPLEGIA AND SENSORY CHANGE. PATIENT WAS TREATED WITH MECHANICAL THROMBECTOMY ON (B)(6) 2024 AND WAS FOUND TO HAVE THROMBUS AT THE BRANCH OF RIGHT INNOMINATE ARTERY. INVESTIGATOR ASSESSMENT OF POSSIBLY RELATED TO DEVICE, UNDETERMINED IF RELATED TO THORAFLEX HYBRID OR RELAYPRO NBS SPECIFICALLY. PREVIOUS ADVERSE EVENT OF ANEURYSM EXPANSION, DYSPHONIA AND RIGHT VENT DYSFUNCTION." PATIENT OUTCOME: "RESOLVED (B)(6) 2024 - REMAINS IN STUDY FOLLOW UP."

    Description of Event or Problem · 0

    "IS THIS EVENT RELATED TO DEVICE FAILURE / DEFICIENCY? POSSIBLY IS THIS EVENT RELATED TO THE PROCEDURE? NO IS THIS EVENT RELATED TO A PRE-EXISTING CONDITION? NO WAS SURGICAL INTERVENTION REQUIRED. ADMITTED TO OUTSIDE HOSPITAL ON (B)(6) 2024 WITH LEFT SIDED HEMIPLEGIA AND SENSORY CHANGE. PATIENT WAS TREATED WITH MECHANICAL THROMBECTOMY ON (B)(6) 2024 AND WAS FOUND TO HAVE THROMBUS AT THE BRANCH OF RIGHT INNOMINATE ARTERY. INVESTIGATOR ASSESSMENT OF POSSIBLY RELATED TO DEVICE, UNDETERMINED IF RELATED TO THORAFLEX HYBRID OR RELAYPRO NBS SPECIFICALLY. PREVIOUS ADVERSE EVENT OF ANEURYSM EXPANSION, DYSPHONIA AND RIGHT VENT DYSFUNCTION." PATIENT OUTCOME: "RESOLVED (B)(6) 2024 - REMAINS IN STUDY FOLLOW UP."

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    507698 RELAY PRO NBS THORACIC STENT-GRAFT SYSTEM STENT, ENDOVASCULAR GRAFT, AORTIC MIH BOLTON MEDICAL, INC. 2306290192 00843576150614

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Male Hospitalization| O| R