FDA Adverse Event Death Summary report: N

ANEURX ILIAC EXT CUFF SG W/XCELERANT DEL SYSTEM

MDR report key: 5215336 · Received November 10, 2015

Report

Report Number
2953200-2015-01955
Event Type
Death
Date Received
November 10, 2015
Date of Event
October 17, 2015
Report Date
October 17, 2015
Manufacturer
MEDTRONIC CARDIOVASCULAR SANTA ROSA
Product Code
MIH
PMA / PMN Number
P990020
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

AN ANEURX STENT GRAFT SYSTEM WAS IMPLANTED IN A PATIENT FOR THE ENDOVASCULAR TREATMENT OF AN ABDOMINAL AORTIC ANEURYSM. IT WAS REPORTED THAT THE PATIENT HAD PRESENTED EMERGENTLY WITH A CONTAINED ANEURYSM RUPTURE. AT THAT TIME THE PHYSICIAN STATED THAT ON CT IT WAS THOUGHT THERE WAS A FRACTURE IN THE ILIAC LIMB ON LEFT SIDE THAT CAUSED THE RUPTURE. THE DECISION WAS MADE TO TREAT THE PATIENT. ACCESS WAS OBTAINED AND AN ANGIOGRAM REVEALED THAT THERE WAS NO STENT FRACTURE AND THE LEFT ILIAC HAD BECOME ANEURYSMAL DISTAL TO STENT GRAFT AND HAD RUPTURED. A 16X13X156 ENDURANT STENT GRAFT WAS PLACED IN THE EXISTING GRAFT EXTENDING INTO LEFT EXTERNAL ILIAC. THIS SUCCESSFULLY STOPPED THE LEAKING ANEURYSM. THE PHYSICIAN NOTED ON ANGIOGRAM THAT THE RIGHT ILIAC ARTERY HAD BECOME ANEURYSMAL DISTAL TO THE STENT GRAFT ALSO, SO EXTENDED INTO THE RIGHT EXTERNAL WITH A 16X13X93 ENDURANT STENT GRAFT. THE PATIENT REFUSED BLOOD PRODUCTS AND IN POST-OP DEVELOPED SEVERE ANEMIA. THE PATIENT HAD A CARDIAC ARREST AND EXPIRED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
745675 ANEURX ILIAC EXT CUFF SG W/XCELERANT DEL SYSTEM SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT MIH MEDTRONIC CARDIOVASCULAR SANTA ROSA YRIRHXC16115

Patients

Seq Age Sex Outcome Treatment
1 00091 YR Death| R