MAUDE Adverse Event Report: BOSTON SCIENTIFIC NEUROMODULATION CORPORATION INFINION? CX; STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF

Model Number	SC-2317-70
Medical Device Problem Code	High impedance (1291)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	05/04/2026
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Block b3: approximated based on the date the manufacturer became aware of the event.D2b pro code (product code): qrb.Additional suspect medical device components involved in the event: model number/catalog number: sc-2317-70.Serial number: (b)(6).Batch/lot number: (b)(6).Model/catalog description: infinion cx lead kit, 70cm.Unique identifier (udi) #: (b)(4).Model number/catalog number: sc-1160.Batch/lot number: (b)(6).Serial number: (b)(6).Model/catalog description: spectra wavewriter ipg kit.Unique identifier (udi) #: (b)(4).
Event or Problem Description
It was reported that the leads had high impedances.The patient underwent a lead replacement procedure and was doing well postoperatively.The explanted devices were not returned.
Event or Problem Description
It was reported that the leads had high impedances.The patient underwent a lead replacement procedure and was doing well postoperatively.The explanted devices were not returned.
Additional Manufacturer Narrative
Investigation results, media review, device analysis the device was not returned for analysis; therefore, a technical analysis could not be performed.Device history record it was confirmed these devices met manufacturing specification prior to distribution and there were no manufacturing deviations which could have contributed to the reported event.Investigation conclusion based on a thorough review of the reported complaint, boston scientific has assigned an investigation conclusion code of cause not established block b3: approximated based on the date the manufacturer became aware of the event.D2b pro code (product code): qrb additional suspect medical device components involved in the event: model number/catalog number: sc-2317-70 serial number: (b)(6) batch/lot number: 5074654 model/catalog description: infinion cx lead kit, 70cm unique identifier (udi) #: (b)(4) model number/catalog number: sc-1160 batch/lot number: 338112 serial number: (b)(6) model/catalog description: spectra wavewriter ipg kit unique identifier (udi) #: (b)(4).

• Brand Name: INFINION? CX
• Common Device Name: STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF
• 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: 25336458
• Report Number: 3006630150-2026-03609
• Device Sequence Number: 18560934
• Product Code: LGW
• UDI-Device Identifier: 08714729861638
• UDI-Public: (01)08714729861638(17)200629(10)5070944
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: P030017
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2018
• Device Explanted Year: 2026
• 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
• Report Date (Section B): 07/16/2026

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?: Yes
• Operator of Device: Lay User/Patient
• Device Expiration Date: 06/29/2020
• Device Model Number: SC-2317-70
• Device Catalogue Number: SC-2317-70
• Device Lot Number: 5070944
• 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: 05/04/2026
• Supplement Date Received by Manufacturer: 06/19/2026
• Initial Report FDA Received Date: 05/29/2026
• Supplement Report FDA Received Date: 07/16/2026
• Date Device Manufactured: 06/30/2018
• 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: 77 YR
• Patient Sex: Male