FDA Adverse Event Injury Summary report: N

GORE TAG THORACIC ENDOPROSTHESIS

MDR report key: 3111779 · Received April 30, 2013

Report

Report Number
2017233-2013-00269
Event Type
Injury
Date Received
April 30, 2013
Date of Event
October 4, 2010
Report Date
April 3, 2013
Manufacturer
W.L. GORE & ASSOCIATES
Product Code
MIH
PMA / PMN Number
P040043
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

RESULTS: THE REVIEW OF THE MANUFACTURING PAPERWORK VERIFIED THAT THIS LOT MET ALL PRE-RELEASE SPECIFICATIONS. ACCORDING TO THE INSTRUCTIONS FOR USE, KEY ANATOMIC ELEMENTS THAT MAY AFFECT SUCCESSFUL EXCLUSION OF THE ANEURYSM INCLUDE SEVERE NECK ANGULATION. AS REPORTED, NECK ANGULATION WAS 125 DEGREES.

Description of Event or Problem · 1

ON (B)(6) 2009, THIS PATIENT UNDERWENT A PROCEDURE USING TWO GORE TAG THORACIC ENDOPROSTHESIS TO TREAT A THORACIC ANEURYSM. TG3420/06550693 WAS FIRST IMPLANTED PROXIMALLY, AND THEN TG3715/06490729 WAS IMPLANTED DISTALLY. THE LENGTH OF THE DISTAL LANDING ZONE WAS ABOUT 20MM. THE DISTAL NECK ANGULATION WAS 125 DEGREES. THE ANEURYSM WAS 76MM. IT WAS REPORTED THAT UPON DEPLOYMENT, THE TAG DEVICE MOVED PROXIMALLY APPROXIMATELY 1.5CM. ON (B)(6) 2009, COMPUTED TOMOGRAPHY IMAGING SHOWED A DISTAL TYPE 1 ENDOLEAK. ON (B)(6) 2009, A TG3710/04889003 WAS IMPLANTED TO REPAIR THE DISTAL TYPE 1 ENDOLEAK. ON (B)(6) 2010, 6 MONTH FOLLOW UP COMPUTED TOMOGRAPHY SHOWED NO ENDOLEAK. PLEASE NOTE: THIS REPORT IS ON THE TG3715/06490729 IMPLANTED ON (B)(6) 2009.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
186003 GORE TAG THORACIC ENDOPROSTHESIS MIH / SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT MIH W.L. GORE & ASSOCIATES 06490729

Patients

Seq Age Sex Outcome Treatment
1 75 YR Hospitalization| R IMPLANTED| TG3420/06550693