FDA Adverse Event Malfunction Summary report: N

ENDURANT STENT GRAFT

MDR report key: 23144181 · Received September 25, 2025

Report

Report Number
9612164-2025-04758
Event Type
Malfunction
Date Received
September 25, 2025
Date of Event
June 17, 2024
Report Date
September 25, 2025
Manufacturer
MEDTRONIC IRELAND
Product Code
MIH
PMA / PMN Number
P100021
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

MEDTRONIC RECEIVED THE FOLLOWING INFORMATION FROM A JOURNAL ARTICLE ENTITLED; ¿COMPARISON OF CHIMNEY TECHNIQUE AND SINGLE-BRANCHED STENT GRAFT IN A COHORT OF PATIENTS WITH TYPE B AORTIC DISSECTIONS: A RETROSPECTIVE COHORT STUDY¿ XING Y, ZHU Z, ZOU L, WU J, XU G, XU Y, HE Z, CAO J, LUO C. CARDIOVASC DIAGN THER. 2024 JUN 30;14(3):367-376. DOI: 10.21037/CDT-23-449 A.2 & 3A AVERAGE VALUES MEDTRONIC SUBMITS THIS REPORT TO COMPLY WITH FDA REGULATIONS 21 CFR PARTS 4 AND 803. MEDTRONIC HAS MADE REASONABLE EFFORTS TO PROVIDE AS MUCH RELEVANT INFORMATION AS IS AVAILABLE TO THE COMPANY AS OF THE SUBMISSION DATE OF THIS REPORT. THIS REPORT DOES NOT CONSTITUTE AN ADMISSION OR A CONCLUSION BY FDA, MEDTRONIC, OR ITS EMPLOYEES THAT THE DEVICE, MEDTRONIC, OR ITS EMPLOYEE CAUSED OR CONTRIBUTED TO THE EVENT DESCRIBED IN THE REPORT. ANY REQUIRED FIELDS THAT ARE UNPOPULATED ARE BLANK BECAUSE THE INFORMATION IS CURRENTLY UNKNOWN OR UNAVAILABLE. MEDTRONIC WILL SUBMIT A SUPPLEMENTAL REPORT IF ADDITIONAL RELEVANT INFORMATION BECOMES KNOWN.

Description of Event or Problem · 0

LITERATURE WAS REVIEWED REGARDING ¿COMPARISON OF CHIMNEY TECHNIQUE AND SINGLE-BRANCHED STENT GRAFT IN A COHORT OF PATIENTS WITH TYPE B AORTIC DISSECTIONS: A RETROSPECTIVE COHORT STUDY¿ THE TIME FRAME OF THIS STUDY WAS OVER A TWO-YEAR PERIOD. ENDURANT AND NON-MDT STENT GRAFTS WERE IMPLANTED IN THE ENDOVASCULAR TREATMENT OF TYPE B AORTIC DISSECTIONS. DURING THESE TEVAR¿S, THE LSA WAS ALSO RECONSTRUCTED WITH NON-MDT STENTS. AMONG THE PATIENT POPULATION THE FOLLOWING MALFUNCTIONS OCCURRED: TYPE I ENDOLEAK, UNKNOWN ENDOLEAK NO FURTHER INFORMATION WAS PROVIDED PERTAINING TO MEDTRONIC PRODUCTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1613684 ENDURANT STENT GRAFT SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TR MIH MEDTRONIC IRELAND UNK-CV-SR-ENDURANT

Patients

Seq Age Sex Outcome Treatment
1 56 YR Male