FDA Adverse Event Injury Summary report: N

VALIANT STENT GRAFT

MDR report key: 10394768 · Received August 12, 2020

Report

Report Number
9612164-2020-02957
Event Type
Injury
Date Received
August 12, 2020
Date of Event
February 5, 2020
Report Date
August 12, 2020
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

MEDTRONIC RECEIVED THE FOLLOWING INFORMATION FROM A JOURNAL ARTICLE ENTITLED; ENDOVASCULAR TREATMENT FOR AORTIC ARCH PATHOLOGIES: CHIMNEY, ON-THE-TABLE FENESTRATION, AND IN-SITU FENESTRATION TECHNIQUES. CHANG S, FAN B, LUO M, LI Q, FANG K, LI M, LI X, HE H, WANG TUN, YANG C, XUE Y, GAO H <(>&<)> ZHAO J. JOURNAL OF THORACIC DISEASE 2020;12(4):1437-1448 HTTP://DX.DOI.ORG/10.21037/JTD.2020.03.10. (B)(4). IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

VALIANT STENT GRAFTS AND NON MDT STENT GRAFTS WERE IMPLANTED IN PATIENTS IN TEVAR PROCEDURES COMBINED WITH ADAPTED TECHNIQUES INCLUDING CHIMNEY AND ON-THE-TABLE FENESTRATION TECHNIQUES. THE FOLLOWING MALFUNCTIONS WERE OBSERVED; TYPE IA ENDOLEAK, TYPE II ENDOLEAK THE FOLLOWING ADVERSE EVENTS WERE OBSERVED; OCCLUSION, STROKE, ISCHEMIA, RENAL FAILURE, CARDIAC EVENTS, DISSECTION AND RE-INTERVENTION. PATIENT DEATHS WERE ALSO REPORTED BUT THERE WAS NO CAUSAL LINK THAT THE VALIANT STENT GRAFTS CAUSED OR CONTRIBUTED TO THESE DEATHS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
861849 VALIANT STENT GRAFT SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT MIH MEDTRONIC IRELAND UNK-CV-SR-VALIANT

Patients

Seq Age Sex Outcome Treatment
1 58 YR Other| R