FDA Adverse Event Malfunction Summary report: N

TALENT AAA

MDR report key: 7685410 · Received July 13, 2018

Report

Report Number
2953200-2018-01017
Event Type
Malfunction
Date Received
July 13, 2018
Date of Event
April 26, 2018
Report Date
October 5, 2018
Manufacturer
MEDTRONIC IRELAND
Product Code
MIH
PMA / PMN Number
P070027
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

MEDTRONIC RECEIVED THE FOLLOWING INFORMATION FROM THE JOURNAL ARTICLE ENTITLED; OPEN THORACIC AND THORACO-ABDOMINAL AORTIC REPAIR AFTER PRIOR ENDOVASCULAR THERAPY PAULA R. KESCHENAU, SHIRLEY KETTING, BAREND MEES, MOHAMMAD E. BARBATI, JOCHEN GROMMES, ALEXANDER GOMBERT, GEERT WILLEM H. SCHURINK, DROSOS KOTELIS, MICHAEL J. JACOBS EUR J VASC ENDOVASC SURG (2018) 56, 57-67, DOI.ORG/10.1016/J.EJVS.2018.03.015. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Additional Manufacturer Narrative · 1

IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

UNKNOWN MEDTRONIC STENT GRAFT SYSTEM WERE IMPLANTED INTO PATIENTS FOR EVAR,TEVAR AND FEVAR TREATMENTS ON UNKNOWN DATES. THE LIST OF EVENTS THAT OCCURRED ARE THE FOLLOWING; MALFUNCTION; TYPE IA ENDOLEAK, TYPE IB ENDOLEAK, PERSISTING FALSE LUMEN PERFUSION, DEVICE FRACTURE/DISLOCATION. INITIAL ENDOGRAFT MISPLACEMENT, MIGRATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
528122 TALENT AAA SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT MIH MEDTRONIC IRELAND

Patients

Seq Age Sex Outcome Treatment
1 58 YR