TRANSEND GUIDEWIRE
Report
- Report Number
- 2939204-2011-00097
- Event Type
- Injury
- Date Received
- March 9, 2011
- Report Date
- February 18, 2011
- Manufacturer
- BOSTON SCIENTIFIC - COSTA RICA
- Product Code
- DQX
- PMA / PMN Number
- K964611
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- OTHER
Narratives
THE DEVICE WAS NOT AVAILABLE FOR ANALYSIS. FROM THE INFORMATION PROVIDED THERE WAS NO INDICATION THAT THE DEVICE WAS NOT USED AS IN ACCORDANCE WITH THE LABELING OR THAT THIS CAUSED OR CONTRIBUTED TO THE REPORTED EVENT. ANEURYSM RUPTURE AND NEUROLOGICAL DEFICIT ARE KNOWN AND ANTICIPATED COMPLICATIONS TO THESE TYPES OF PROCEDURES AND ARE NOTED IN THE LABELING. THEREFORE, IT WAS DETERMINED THAT THE REPORTED EVENT WAS AN ANTICIPATED PROCEDURAL COMPLICATION.
EVENT DATE: THE PATIENT UNDERWENT THE PROCEDURE ON (B)(6) 2006, THE EXACT DATE IS UNKNOWN. THE EVENT WAS REPORTED BY THE LAWYER, MR. (B)(6). NO CONTACT DETAILS WERE PROVIDED.
IT WAS REPORTED THAT THE ANEURYSM RUPTURED DURING THE EMBOLIZATION. THE PATIENT HAD SUBSEQUENT 'DYSFUNCTIONS OF UPPER/LOWER EXTREMITIES'. NO FURTHER INFORMATION WAS PROVIDED.
IT WAS REPORTED THAT THE ANEURYSM RUPTURED DURING THE EMBOLIZATION. THE PATIENT HAD SUBSEQUENT 'DYSFUNCTIONS OF UPPER/LOWER EXTREMITIES'. NO FURTHER INFORMATION WAS PROVIDED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TRANSEND GUIDEWIRE | WIRE, GUIDE, CATHETER | DQX | BOSTON SCIENTIFIC - COSTA RICA | M003468020 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other| S | GUIDER CATHETER (BOSTON SCIENTIFIC)| EXCELSIOR SL-10 MICROCATHETER (BOSTON SCIENTIFIC)| GDC-10 360 SOFT COIL (BOSTON SCIENTIFIC)| SENTRY BALLOON CATHETER (BOSTON SCIENTIFIC)| TRANSEND EX 014 GUIDEWIRE (BOSTON SCIENTIFIC) |