MAUDE Adverse Event Report: BOSTON SCIENTIFIC NEUROMODULATION CORPORATION VERCISE GENUS?; STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR

Model Number	DB-1408
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/14/2025
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
B3: approximated based on the date the manufacturer became aware of the event.D2b: additional pro code selection that applies to the indication of this device - .
Event or Problem Description
It was reported that this deep brain stimulation (dbs) device was explanted due to an unknown reason.The location of the device is unknown.No additional adverse patient effects were reported.
Event or Problem Description
It was reported that this deep brain stimulation (dbs) device was explanted due to an unknown reason.The location of the device is unknown.No additional adverse patient effects were reported.Additional information was received stating that this dbs device was electively replaced.The patient underwent an implantable pulse generator (ipg) revision procedure wherein their ipg was explanted and replaced.The ipg was discarded by the facility and will not be returned for analysis.Postoperatively, the patient was doing well.
Additional Manufacturer Narrative
D2b: additional pro code selection that applies to the indication of this device - .
Additional Manufacturer Narrative
The device was not returned for analysis; therefore, a technical analysis could not be performed.A review of the device history record (dhr) confirmed that the device met specification prior to shipping and there were no manufacturing deviations noted that could have contributed to the event reported.Based on a thorough review of the reported complaint, boston scientific has assigned an investigation conclusion code of: unable to exclude device problem.D2b: additional pro code selection that applies to the indication of this device - .
Event or Problem Description
It was reported that this deep brain stimulation (dbs) device was explanted due to an unknown reason.The location of the device is unknown.No additional adverse patient effects were reported.Additional information was received stating that this dbs device was electively replaced.The patient underwent an implantable pulse generator (ipg) revision procedure wherein their ipg was explanted and replaced.The ipg was discarded by the facility and will not be returned for analysis.Postoperatively, the patient was doing well.

• Brand Name: VERCISE GENUS?
• Common Device Name: STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR
• Manufacturer (Section D): BOSTON SCIENTIFIC NEUROMODULATION CORPORATION; 25155 rye canyon loop; valencia CA 91355
• Manufacturer (Section G): BOSTON SCIENTIFIC CORPORATION; cashel road; clonmel ; EI
• Manufacturer Contact: erik sherburne ; 25155 rye canyon loop; valencia, CA 91355 ; 7632920920
• MDR Report Key: 22804967
• Report Number: 3006630150-2025-06488
• Device Sequence Number: 8951293
• Product Code: MHY
• UDI-Device Identifier: 08714729989752
• UDI-Public: (01)08714729989752(17)230412(10)203758
• Combination Product (Y/N): N
• Initial Reporter State: MT
• Initial Reporter Country: US
• PMA/510(K) Number: P150031
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Device Explanted Year: 2025
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 03/27/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Lay User/Patient
• Device Expiration Date: 04/12/2023
• Device Model Number: DB-1408
• Device Catalogue Number: DB-1408
• Device Lot Number: 203758
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/21/2025
• Supplement Date Received by Manufacturer: 08/20/2025; 03/03/2026
• Initial Report FDA Received Date: 08/14/2025
• Supplement Report FDA Received Date: 09/09/2025; 03/30/2026
• Date Device Manufactured: 04/12/2021
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 57 YR
• Patient Sex: Female