FDA Adverse Event Injury Summary report: N

VALIANT STENT GRAFT

MDR report key: 7840817 · Received September 3, 2018

Report

Report Number
9612164-2018-02247
Event Type
Injury
Date Received
September 3, 2018
Date of Event
July 28, 2018
Report Date
September 3, 2018
Manufacturer
MEDTRONIC IRELAND
Product Code
MIH
PMA / PMN Number
P100040
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

TITLE: COMPUTATIONAL INVESTIGATION OF INTERACTION BETWEEN STENT GRAFT AND AORTA IN RETROGRADE TYPE A DISSECTION AFTER THORACIC ENDOVASCULAR AORTIC REPAIR FOR TYPE B AORTIC DISSECTION AUTHOR: TAO MA, MD,A ZHI HUI DONG, MD,A SHENGZHANG WANG, PHD,B ZHUANG YUAN MENG, BD,B YIN YIN CHEN, MD,C AND WEI GUO FU, MD, JOURNAL OF VASCULAR SURGERY (2018) 06.008 DOI.ORG/10.1016/J.JVS.2018.06.008. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

A VALIANT OR A TALENT STENT GRAFT SYSTEM WAS IMPLANTED IN A PATIENT FOR THE ENDOVASCULAR TREATMENT FOR AN AAA ON AN UNKNOWN DATE. IT WAS REPORTED THAT AT AN UNKNOWN DATE AFTER THE IMPLANTATION THE PATIENT DEVELOPED STENT GRAFT INDUCED RETROGRADE TYPE A DISSECTION (RTAD) WITH A NEW TEAR IN THE GREATER AORTIC CURVE. THE PATIENT UNDERWENT OPEN REPAIR OF ASCENDING AORTA AND THE STENT GRAFTING OF DESCENDING AORTA. NO ADDITIONAL CLINICAL SEQUELAE WERE REPORTED AND THE PATIENT WILL BE MONITORED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
681451 VALIANT STENT GRAFT SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT MIH MEDTRONIC IRELAND

Patients

Seq Age Sex Outcome Treatment
1 31 YR Required Intervention