FDA Adverse Event Death Summary report: N

MEDTRONIC VALIANT STENT

MDR report key: 18989995 · Received March 27, 2024

Report

Report Number
MW5153273
Event Type
Death
Date Received
March 27, 2024
Report Date
March 27, 2024
Manufacturer
MEDTRONIC IRELAND
Product Code
MIH
Adverse Event
Yes
Report Source
Voluntary report
Reporter Occupation
UNKNOWN
Health Professional
*

Narratives

Description of Event or Problem · 0

THIS CONSUMER COMPLAINT WAS REGARDING A DEATH AFTER AN IMPLANT OF MEDTRONIC VALIANT STENTS. THE COMPLAINANT LIVES IN CHINA AND STENTS WERE MANUFACTURED IN IRELAND. REFERENCE REPORT: MW5153272.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
721343 MEDTRONIC VALIANT STENT SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT MIH MEDTRONIC IRELAND

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Death