INTRAVASCULAR SHUNT
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
THE EVENT IS CURRENTLY UNDER INVESTIGATION.
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.
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 |