MICROPLEX 10-SYSTEM COIL (MCS)
Report
- Report Number
- 2032493-2009-00024
- Event Type
- Injury
- Date Received
- March 27, 2009
- Date of Event
- February 25, 2009
- Report Date
- February 27, 2009
- Manufacturer
- MICROVENTION, INC.
- Product Code
- HCG
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CO, US
- Reporter Occupation
- PHYSICIAN
Narratives
DEVICE 9 OF 12. COMPLAINT SAMPLE WAS NOT RETURNED FOR EVAL AS IT IS IMPLANTED WITHIN THE PT. ACCESSORY EQUIPMENT USED DURING THIS EMBOLIZATION PROCEDURE CONSISTED OF A VISTA BRITE TIP GUIDING CATHETER MANUFACTURED BY CORDIS CORPORATION, A SL 10 MICROCATHETER, SYNCHRO 2 GUIDEWIRE, AND A SYNCHRO 14 GUIDEWIRE MANUFACTURED BY BOSTON SCIENTIFIC, A HYPERFORM OCCLUSION BALLOON SYSTEM, A SILVERSPEED 14 GUIDEWIRE, AND AN X-PEDION GUIDEWIRE MANUFACTURED BY EV3 NEUROVASCULAR. THE EMBOLIZATION PROCEDURE LASTED FOR 5 1/2 HOURS. IT IS UNLIKELY THAT THE MRI INFARCTS RESULTED FROM EMBOLI GENERATED FROM THE MICROVENTION EMBOLIZATION COILS. THIS IS BECAUSE SOME OF THE MRI INFARCT AREAS WERE SERVED BY ARTERIAL BRANCHES THAT WERE PROXIMAL (RETROGRADE) TO THE ANEURYSM IN WHICH MICROVENTION EMBOLIZATION COILS WERE DEPLOYED.
IT WAS REPORTED THAT A PATIENT PRESENTING WITH HEMIPLEGIA ASSOCIATED WITH PRIOR CEREBRAL ANEURYSM RUPTURE, INCURRED SMALL CEREBRAL INFARCTS VISUALIZED BY MRI, AND A HEADACHE, AFTER TREATMENT OF AN UNRUPTURED POSTERIOR COMMUNICATING (PCOM) ANEURYSM USING MICROVENTION EMBOLIZATION COILS. THE HEADACHE RESOLVED AFTER ADMINISTRATION OF DECADRON, A GLUCOCORTICOSTEROID.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MICROPLEX 10-SYSTEM COIL (MCS) | DEVICE 9 OF 12 - EMBOLIZATION COIL | HCG | MICROVENTION, INC. | 100201HS-V | P0902033 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention| S |