FDA Adverse Event Injury Summary report: N

VALIANT STENT GRAFT

MDR report key: 11854250 · Received May 20, 2021

Report

Report Number
9612164-2021-01987
Event Type
Injury
Date Received
May 20, 2021
Date of Event
October 18, 2020
Report Date
May 20, 2021
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; OUTCOMES OF ENDOVASCULAR STENT GRAFT REPAIR FOR PENETRATING AORTIC ULCERS WITH OR WITHOUT INTRAMURAL HEMATOMA JIANG X, PAN T, ZOU L, CHEN B, JIANG J, SHI Y, MA T, LIN C, GUO D, XU X, YANG J, SHI Z, ZHU T, DONG Z, FU W JOURNAL OF VASCULAR SURGERY. 2021 MAY;73(5):1541-1548. DOI: 10.1016/J.JVS.2020.10.022 IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

A VALIANT STENT GRAFT WAS IMPLANTED IN THE ENDOVASCULAR TREATMENT OF A PENETRATING AORTIC ULCER (PAU) AND INTRAMURAL HEMATOMA (IMH) ON AN UNKNOWN DATE. IT WAS REPORTED AT THE 24 MONTH FOLLOW-UP, THE PATIENT WAS DIAGNOSED WITH ASYMPTOMATIC DISTAL STENT-INDUCED NEW ENTRY (SINE) TEAR. THIS WAS THEN MEDICAL MANAGED. NO CAUSE WAS REPORTED. NO ADDITIONAL CLINICAL SEQUELAE WERE PROVIDED AND THE PATIENT WILL BE MONITORED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
752654 VALIANT STENT GRAFT SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT MIH MEDTRONIC IRELAND UNK-CV-SR-VALIANT

Patients

Seq Age Sex Outcome Treatment
1 70 YR Other