MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-01-23 for VERCISE GEVIA DB-1200-S manufactured by Boston Scientific Neuromodulation.
[176204073]
Date of death is december 2019, the exact date is unknown.
Patient Sequence No: 1, Text Type: N, H10
[176204074]
A report was received that the patient passed away one week after being implanted with the deep brain stimulation system. The physician stated that the patients death was due to a pulmonary embolism and not due to the device or to cranial artery. The exact date of death is unknown.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3006630150-2020-00165 |
MDR Report Key | 9624801 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-01-23 |
Date of Report | 2020-01-23 |
Date of Event | 2019-12-27 |
Date Mfgr Received | 2020-01-03 |
Device Manufacturer Date | 2019-10-08 |
Date Added to Maude | 2020-01-23 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 0 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | TALAR TAHMASIAN |
Manufacturer Street | 25155 RYE CANYON LOOP |
Manufacturer City | VALENCIA CA 91355 |
Manufacturer Country | US |
Manufacturer Postal | 91355 |
Manufacturer Phone | 6619494863 |
Manufacturer G1 | BOSTON SCIENTIFIC CORPORATION |
Manufacturer Street | CASHEL ROAD |
Manufacturer City | CLONMEL |
Manufacturer Country | EI |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | VERCISE GEVIA |
Generic Name | STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS |
Product Code | NHL |
Date Received | 2020-01-23 |
Model Number | DB-1200-S |
Catalog Number | DB-1200-S |
Lot Number | 740027 |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BOSTON SCIENTIFIC NEUROMODULATION |
Manufacturer Address | 25155 RYE CANYON LOOP VALENCIA CA 91355 US 91355 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Death | 2020-01-23 |