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

Model Number	DB-3128-55B
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Erosion (1750); Unspecified Infection (1930)
Date of Event	03/11/2025
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that the deep brain stimulation (dbs) patient experienced erosion with a potential infection at the dbs implant site.The patient underwent a procedure wherein the dbs lead extension was removed.The physicians assessment was thought to believe the lead extension has a sharp edge at the connection site causing the erosion, however it is unknown which tail end is being reported.No further information has been provided despite good faith efforts.
Additional Manufacturer Narrative
Block d2b: additional pro codes nhl, pjs.Block b3: approximated based on the date the manufacturer became aware of the event.Additional suspect medical device components involved in the event: product family: dbs-ipg-r-mri, upn: m365db12160, model: db-1216, serial: (b)(6), batch: 753139.Product family: dbs-linear leads upn: m365db2202450, model: db-2202-45, serial: n/i, batch: n/i.
Event or Problem Description
It was reported that the deep brain stimulation (dbs) patient experienced erosion with a potential infection at the dbs implant site.The patient underwent a procedure wherein the dbs lead extension was removed.The physicians assessment was thought to believe the lead extension has a sharp edge at the connection site causing the erosion, however it is unknown which tail end is being reported.No further information has been provided despite good faith efforts.Additional information provided confirmed the dbs devices remain implanted and continue to deliver therapy.The patient had undergone a procedure wherein a wound washout was completed before reclosing the incision.It was confirmed there was no infection present however the patient was prescribed anti-biotics per the physicians assessment.The patient is doing fine.
Additional Manufacturer Narrative
This report is being submitted as additional information was received in block b5.Additional suspect medical device components involved in the event: product family: dbs-ipg-r-mri.Upn: m365db12160.Model: db-1216.Serial: (b)(6).Batch: 753139.Udi#: (b)(4).Product family: dbs-linear leads.Upn: m365db2202450.Model: db-2202-45.Serial: (b)(6).Batch: 7112015.Udi#: (b)(4).This report is being submitted to correct the field operator of device block d5, patient code block h6.

• Brand Name: VERCISE
• 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; road 698, lot no. 12; dorado PR 00646 -260; * 00646-2602
• Manufacturer Contact: erik sherburne ; 25155 rye canyon loop; valencia, CA 91355 ; 7632920920
• MDR Report Key: 21801918
• Report Number: 2124215-2025-21799
• Device Sequence Number: 18399899
• Product Code: MHY
• UDI-Device Identifier: 00191506023577
• UDI-Public: 00191506023577
• Combination Product (Y/N): N
• Initial Reporter State: MN
• Initial Reporter Country: US
• PMA/510(K) Number: P150031
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2024
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 05/12/2025

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?: Yes
• Operator of Device: Lay User/Patient
• Device Expiration Date: 03/05/2026
• Device Model Number: DB-3128-55B
• Device Catalogue Number: DB-3128-55B
• Device Lot Number: 5002498
• 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: 03/13/2025
• Supplement Date Received by Manufacturer: 04/17/2025
• Initial Report FDA Received Date: 04/08/2025
• Supplement Report FDA Received Date: 05/12/2025
• Date Device Manufactured: 03/05/2024
• 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: 68 YR
• Patient Sex: Female