VERCISE GEVIA DB-1200-S

MAUDE Adverse Event Report

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.

Event Text Entries

[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


MAUDE Entry Details

Report Number3006630150-2020-00165
MDR Report Key9624801
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-01-23
Date of Report2020-01-23
Date of Event2019-12-27
Date Mfgr Received2020-01-03
Device Manufacturer Date2019-10-08
Date Added to Maude2020-01-23
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag0
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactTALAR TAHMASIAN
Manufacturer Street25155 RYE CANYON LOOP
Manufacturer CityVALENCIA CA 91355
Manufacturer CountryUS
Manufacturer Postal91355
Manufacturer Phone6619494863
Manufacturer G1BOSTON SCIENTIFIC CORPORATION
Manufacturer StreetCASHEL ROAD
Manufacturer CityCLONMEL
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVERCISE GEVIA
Generic NameSTIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS
Product CodeNHL
Date Received2020-01-23
Model NumberDB-1200-S
Catalog NumberDB-1200-S
Lot Number740027
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC NEUROMODULATION
Manufacturer Address25155 RYE CANYON LOOP VALENCIA CA 91355 US 91355


Patients

Patient NumberTreatmentOutcomeDate
101. Death 2020-01-23

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