FDA Adverse Event Injury Summary report: N

ENDURANT II

MDR report key: 4090348 · Received September 15, 2014

Report

Report Number
2953200-2014-01831
Event Type
Injury
Date Received
September 15, 2014
Date of Event
August 5, 2014
Report Date
August 21, 2014
Manufacturer
MEDTRONIC IRELAND
Product Code
MIH
PMA / PMN Number
P100021
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). CONCLUSION: PRE IMPLANT RUPTURE.

Description of Event or Problem · 1

AN ENDURANT STENT GRAFT SYSTEM WAS IMPLANTED FOR THE ENDOVASCULAR TREATMENT OF A RUPTURED ABDOMINAL AORTIC ANEURYSM. IT WAS REPORTED THAT AFTER THE PROCEDURE (SAME DAY), THE PATIENT WAS COMPLAINING OF LEFT LEG PAIN. A CT SCAN WAS PERFORMED AND THE PATIENT¿S LEFT COMMON ILIAC WAS OCCLUDED AND THE RIGHT COMMON ILIAC SIZE WAS DIMINISHED AT PATIENT¿S ORIGINAL BIFURCATION. THE PHYSICIAN PERFORMED A THROMBECTOMY HOWEVER, WAS ONLY ABLE TO REMOVE CLOT FROM THE EXTERNAL ILIAC TO FEMORAL ARTERY AT ACCESS SITE. THE PHYSICIAN WAS UNABLE TO ACCESS THE LEFT COMMON ILIAC AND DURING THIS PROCESS CREATED A DISSECTED AREA IN THE LEFT DISTAL EXTERNAL ILIAC AND PLACED A VIABAHN STENT (7MM X 10CM) IN THE LEFT EXTERNAL ILIAC AND UPON PERFORMING A RETROGRADE ANGIOGRAM, THE LEFT HYPOGASTRIC ARTERY REMAINED OPEN. THE PHYSICIAN IMPLANTED AN ICAST STENT (10MM X 38MM) AT THE NARROW AREA ON THE RIGHT COMMON ILIAC AND THE AREA INCREASED FROM 7MM TO 10MM. RETROGRADE ANGIOGRAM WAS PERFORMED AND THE VESSEL WAS PERFUSING WELL. THE PHYSICIAN THEN PERFORMED A FEM-FEM BYPASS WITHOUT ISSUES. NO CLINICAL SEQUELAE WERE REPORTED AND THE PATIENT IS FINE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
568181 ENDURANT II SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT MIH MEDTRONIC IRELAND V04039238

Patients

Seq Age Sex Outcome Treatment
1 00065 YR Required Intervention