MATRIX2 STANDARD 360 SR COIL
Report
- Report Number
- 2939204-2008-00586
- Event Type
- Injury
- Date Received
- November 19, 2008
- Date of Event
- September 20, 2008
- Report Date
- November 4, 2008
- Manufacturer
- NEUROVASCULAR, BOSTON SCIENTIFIC CORPORATION
- Product Code
- HCG
- PMA / PMN Number
- K050700
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- PHYSICIAN
Narratives
FOR NO ALLEGATION OF PRODUCT MALFUNCTION OR NON CONFORMANCE CONTRIBUTING TO THE REPORTED EVENT. ADDITIONAL INFORMATION WAS RECEIVED FROM THE USER FACILITY. THE PHYSICIAN DID NOT EXPERIENCE ANY ISSUES WITH THE PREPARATION, DEPLOYMENT, OR DETACHMENT OF ANY OF THE COILS AND THE COILS WERE USED IN ACCORDANCE WITH THE APPROPRIATE DIRECTIONS FOR USE. THE PHYSICIAN DID NOT ALLEGE ANY MALFUNCTION OR NON CONFORMANCE AGAINST THE COILS USED.
APPROXIMATELY TEN DAYS AFTER THE SUCCESSFUL EMBOLIZATION OF A BASILAR-SUPERIOR CEREBELLAR ARTERY ANEURYSM, THE PATIENT REPORTED EXPERIENCING HALLUCINATIONS AND NARROWING OF THE FIELD OF VISION. THE PATIENT DID NOT HAVE ANY NERVE COMPRESSION, INCREASED PRESSURE IN THE EYE OR ISCHEMIA. THE PHYSICIAN NOTED THERE WERE MULTIPLE HIGH SIGNALS AROUND THE ANEURYSM ON THE MAGNETIC RESONANCE IMAGING (MRI) SCAN. THE PHYSICIAN BELIEVES THAT THE VISUAL DISTURBANCES WERE AN INFLAMMATORY REACTION AFTER THE COIL EMBOLIZATION. IT IS UNKNOWN IF THE VISUAL DISTURBANCES HAVE RESOLVED OR IF THE PHYSICIAN TOOK ANY ACTION TO TREAT THE SYMPTOMS. THE PHYSICIAN REPORTED TO BE TAKING A "WAIT AND SEE APPROACH".
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MATRIX2 STANDARD 360 SR COIL | (HCG) DETACHABLE COIL | HCG | NEUROVASCULAR, BOSTON SCIENTIFIC CORPORATION | 492123-SR | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other | AND AN ECHELON MICROCATHETER (EV3)| SIXTEEN MATRIX2 COILS| AN EXCELSIOR SL10 MICROCATHETER| ELEVEN GDC COILS (BOSTON SCIENTIFIC) |