FDA Adverse Event Death Summary report: N

GORE EXCLUDER AAA ENDOPROSTHESIS

MDR report key: 2632503 · Received June 22, 2012

Report

Report Number
2017233-2012-00425
Event Type
Death
Date Received
June 22, 2012
Date of Event
May 29, 2012
Report Date
June 5, 2012
Manufacturer
W.L. GORE & ASSOCIATES
Product Code
MIH
PMA / PMN Number
P020004
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THE REVIEW OF THE MFG PAPERWORK VERIFIED THAT THIS LOT MET ALL PRE-RELEASE SPECS. ADD'L DEVICES: 9808890/PXC01400, 9665889/PXC231000, 9882819/PXC201000, 9654251/PXC201200.

Description of Event or Problem · 1

ON (B)(6) 2012, THE PT COMPLAINED OF BELLY PAIN AND A COMPUTED TOMOGRAPHY ANGIOGRAPHY REVEALED AN ABDOMINAL AORTIC ANEURYSM AS WELL AS BILATERAL ILIAC ANEURYSMS. ON (B)(6) 2012, THE PT UNDERWENT REPAIR OF THE ABDOMINAL AORTIC ANEURYSM AND BILATERAL ILIAC ANEURYSMS AND WAS IMPLANTED WITH FIVE GORE EXCLUDER AAA ENDOPROSTHESES. THE PT TOLERATED THE PROCEDURE. ALL ARTERIES APPEARED FINE ON THE FINAL ANGIO. ON (B)(6) 2012, AFTER THE PROCEDURE, THE PT WENT INTO HYPOVOLEMIC SHOCK AND UNDERWENT AN EXPLORATORY LAPAROTOMY. THE PT'S LEFT ILIAC ARTERY WAS RUPTURED. THE PT EXPIRED DUE TO THE RUPTURED ARTERY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GORE EXCLUDER AAA ENDOPROSTHESIS MIH/SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT MIH W.L. GORE & ASSOCIATES 10097868

Patients

Seq Age Sex Outcome Treatment
1 88 YR Death SODIUM CHLORIDE| ASPIRIN| GLUCOSATE SODIUM| LABETALOL| BUPROPION| BENADRYL| OMEPRAZOLE| MAGNESIUM HYDROXIDE| LOSARTAN| TYLENOL| MORPHINE