FDA Adverse Event Malfunction Summary report: N

INTRAVASCULAR SHUNT

MDR report key: 3241676 · Received July 22, 2013

Report

Report Number
3008500478-2013-00479
Event Type
Malfunction
Date Received
July 22, 2013
Date of Event
June 11, 2013
Report Date
June 27, 2013
Manufacturer
EDWARDS LIFESCIENCES
Product Code
DWF
PMA / PMN Number
K990396
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE EVENT IS CURRENTLY UNDER INVESTIGATION.

Additional Manufacturer Narrative · 1

EVALUATION: THE CUSTOMER REPORTED THAT THERE WAS A BIG POINT OF GLUE ON THE DEVICE WAS CONFIRMED. AN EXCESSIVE USE OF ADHESIVE APPEARED IN THE MIDDLE OF THE SHUNT SHAFT THE DEFECT WAS CONFIRMED, AND A MANUFACTURING DEFECT WAS CONFIRMED. THE ROOT CAUSE IS THAT EXCESS ADHESIVE WAS ADDED TO THE SHUNT DURING THE MANUFACTURING OF THE DEVICE. A SUPPLIER AND EDWARDS¿S CORRECTIVE ACTION HAVE BEEN OPEN AND ARE CURRENTLY UNDER INVESTIGATION. A PRODUCT RECALL HAS BEEN INITIATED. THE DEVICE USE ALIGNED WITH THE INTENDED USE OF THE DESIGN. THE LABELING AND IFU CONTAIN ADEQUATE WARNINGS A PRODUCT RECALL HAS BEEN INITIATED DUE TO THESE COMPLAINTS. THE LOT HISTORY WAS REVIEWED, AND THERE WERE NO RELATED NCRS. FROM JULY 01, 2011 TO JULY 29, 2013 THE COMPLAINT TREND WAS FOUND TO BE OUT OF CONTROL. TRENDS WILL CONTINUE TO BE MONITORED THROUGH EDWARDS¿S QUALITY SYSTEMS.

Description of Event or Problem · 1

IT WAS REPORTED THAT ON THE INTRAVASCULAR SHUNTS "IT WAS FOUND DURING USE THAT EXCESSIVE THE AMOUNT OF ADHESIVE WAS APPLIED ON THE SHAFT WHERE THE TETHER WAS ATTACHED AND BECAME LIKE A LUMP."

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
341523 INTRAVASCULAR SHUNT CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS DWF EDWARDS LIFESCIENCES IVS1512 59409889

Patients

Seq Age Sex Outcome Treatment
1