FDA Adverse Event Death Summary report: N

ENDURANT STENT GRAFT

MDR report key: 13257085 · Received January 14, 2022

Report

Report Number
9612164-2022-00213
Event Type
Death
Date Received
January 14, 2022
Date of Event
November 1, 2021
Report Date
January 14, 2022
Manufacturer
MEDTRONIC IRELAND
Product Code
MIH
PMA / PMN Number
P100021
Adverse Event
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;SAFETY AND DURABILITY OF SINGLE-STAGE TYPE I HYBRID TOTAL AORTIC ARCH REPAIR FOR EXTENSIVE AORTIC ARCH DISEASE: EARLY- AND LONG-TERM CLINICAL OUTCOMES FROM A SINGLE CENTER AND OUR 10-YEAR OF EXPERIENCE ZHANG B, WEI Y, LIU Y, LIN H, LIANG S, DUN Y, YU C, QIAN X, GUO H, SUN X JOURNAL OF THORACIC DISEASE 2021;13(11):6230-6239 HTTP://DX.DOI.ORG/10.21037/JTD-20-3479. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 0

ENDURANT , VALIANT CAPTIVIA STENT GRAFTS AND NON MDT STENT GRAFTS WERE IMPLANTED IN THE ENDOVASCULAR TREATMENT OF SINGLE-STAGE TYPE I HYBRID TOTAL AORTIC ARCH REPAIR. TYPE I HYBRID TOTAL AORTIC ARCH REPAIR WAS DEFINED AS SURGICAL TOTAL SUPRA-ARCH DEBRANCHING AND ZONE 0 STENT GRAFT DEPLOYMENT TO EXCLUDE THE ENTIRE DISEASED AORTIC ARCH. THE PATIENTS EXPERIENCED VARIOUS AORTIC PATHOLOGIES INCLUDING ANEURYSMS, DISSECTIONS AND AORTIC ULCERS. A PATIENT PRESENTED AT 2 MONTHS WITH A SUDDEN AORTIC RUPTURE. THE PATIENT EXPIRED SUDDENLY WITHOUT EMERGENCY TREATMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
806559 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 Other| D