FDA Adverse Event Injury Summary report: N

GORE TEX VASCULAR GRAFT

MDR report key: 3315688 · Received August 21, 2013

Report

Report Number
2017233-2013-00576
Event Type
Injury
Date Received
August 21, 2013
Date of Event
May 11, 2013
Report Date
July 22, 2013
Manufacturer
W.L. GORE & ASSOCIATES
Product Code
DSY
PMA / PMN Number
K802095
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

NO TESTING METHODS PERFORMED (NO LOT NUMBER REPORTED). THE ARTICLE CONCLUDED, "WE FOUND THAT A CHILD'S ANATOMY HAS AN IMPACT ON THE OCCURRENCE OF POSTOPERATIVE IN-HOSPITAL SHUNT OCCLUSION. THE PRESENCE OF SMALL PULMONARY ARTERIES MAY HEIGHTEN THE INCIDENCE OF POSTOPERATIVE SHUNT OCCLUSION EITHER BECAUSE OF TECHNICAL ISSUES OR BY INCREASING THE RESISTANCE TO BLOOD FLOW THROUGH THE SHUNT." NOTE: TWELVE REPORTED PEDIATRIC SHUNT OCCLUSIONS WERE REPORTED IN THE ARTICLE.

Description of Event or Problem · 1

DURING AN ARTICLE REVIEW ("IN-HOSPITAL SHUNT OCCLUSION IN INFANTS UNDERGOING A MODIFIED BLALOCK-TAUSSIG SHUNT." ANNALS OF THORACIC SURGERY 2013; 96:176-82, AUTHORS: NINA A. GUZZETTA, MD, GREGORY S. FOSTER, BS, NAVYATA MRUTHINTI, MPH, PATRICK D. KILGORE, MS, BRUCE E. MILLER, MD, AND KIRK R. KANTER, MD), A RETROSPECTIVE REVIEW BETWEEN MARCH 1, 2005, AND DECEMBER 31 IDENTIFIED 207 PTS WHICH RECEIVED A MODIFIED BLALOCK-TAUSSIG SHUNT. A (B)(6) PT WAS IMPLANTED WITH A 3.5 MM SHUNT. THE SHUNT OCCLUDED 12 HOURS POST IMPLANT. THE PT HAD A MEDIASTINAL EXPLORATION IN ICU AND THE SHUNT STOPPED. THE PHYSICIAN FINDINGS WERE AS FOLLOWS: "ACUTE EPISODE OF DESATURATION UNRESPONSIVE TO TREATMENT, ECHO SUGGESTED THROMBUS; POST-ANGIOGRAM SHOWED PATENT SHUNT WITH RESIDUAL THROMBUS LPA."

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
406921 GORE TEX VASCULAR GRAFT DSY/PROSTHESIS, VASCULAR GRAFT DSY W.L. GORE & ASSOCIATES

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention