FDA Adverse Event Injury Summary report: N

VALIANT STENT GRAFT

MDR report key: 11861996 · Received May 21, 2021

Report

Report Number
9612164-2021-02012
Event Type
Injury
Date Received
May 21, 2021
Date of Event
October 19, 2019
Report Date
May 21, 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 NOTIFICATION OF A LITERATURE ARTICLE ENTITLED; OUTCOMES OF ENDOVASCULAR STENT GRAFT REPAIR FOR PENETRATING AORTIC ULCERS WITH OR WITHOUT INTRAMURAL HEMATOMA XIAOLANG JIANG, MD, TIANYUE PAN, MD, LINGWEI ZOU, MD, BIN CHEN, MD, JUNHAO JIANG, MD, YUN SHI, MD, TAO MA, MD, CHANGPO LIN, MD, DAQIAO GUO, MD, XIN XU, MD, JUE YANG, MD, ZHENYU SHI, MD, TING ZHU, MD, ZHIHUI DONG, MD, AND WEIGUO FU, MD SOCIETY FOR VASCULAR SURGERY DOI: HTTPS://DOI.ORG/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 THORACIC STENT GRAFT WAS IMPLANTED IN THE PATIENT FOR THE ENDOVASCULAR TREATMENT OF AN UNKNOWN SIZED PAU WITH ASSOCIATED IMH ON AN UNKNOWN DATE. 12 MONTHS POST IMPLANT, DISTAL SINE WAS OBSERVED. IT WAS REPORTED THE PATIENT WAS ASYMPTOMATIC. NO CAUSE OF THE EVENT WAS REPORTED. NO ADDITIONAL CLINICAL SEQUALA WERE REPORTED AND THE PATIENT WILL BE MONITORED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
759892 VALIANT STENT GRAFT SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT MIH MEDTRONIC IRELAND UNK-CV-SR-VALIANT

Patients

Seq Age Sex Outcome Treatment
1 66 YR Other