MAUDE Adverse Event Report: BOSTON SCIENTIFIC NEUROMODULATION CORPORATION LINEAR? 3-6; STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF

Model Number	SC-2366-70
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	02/25/2026
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Block b3: approximated based on the date the manufacturer became aware of the event additional suspect medical device components involved in the event: model number/catalog number: sc-2366-70, serial number: (b)(6), batch/lot number: 16536641, model/catalog description: linear 3-6 lead 70 cm.Unique identifier (udi) #: (b)(4).Model number/catalog number: sc-2366-70, serial number: (b)(6), batch/lot number: 16536641, model/catalog description: linear 3-6 lead 70 cm, unique identifier (udi) #: (b)(4).
Event or Problem Description
It was reported that the patient with a spinal cord stimulation (scs) device underwent an explant procedure for an unspecified reason.Patient post operatively is doing great.The explanted devices will not return for analysis as no representative was present at the time of event.No additional information is available at this time.
Event or Problem Description
It was reported that the patient with a spinal cord stimulation (scs) device underwent an explant procedure for an unspecified reason.Patient post operatively is doing great.The explanted devices will not return for analysis as no representative was present at the time of event.No additional information is available at this time.
Additional Manufacturer Narrative
The device was not returned to boston scientific for analysis and the complaint as reported was not able to be confirmed.A review of the device history record (dhr) confirmed that the device met specification prior to shipping.No manufacturing deviations were noted that could have contributed to the event reported.Record review revealed no additional information related to the complaint.Therefore, in the absence of device return and analysis the likely root cause could not be established.Block b3: approximated based on the date the manufacturer became aware of the event additional suspect medical device components involved in the event: model number/catalog number: sc-2366-70.Serial number: (b)(6).Batch/lot number: 16536641.Model/catalog description: linear 3-6 lead 70 cm.Unique identifier (udi) #: (b)(4).Model number/catalog number: sc-2366-70.Serial number: (b)(6).Batch/lot number: 16536641.Model/catalog description: linear 3-6 lead 70 cm.Unique identifier (udi) #: (b)(4).
Event or Problem Description
It was reported that the patient with a spinal cord stimulation (scs) device underwent an explant procedure for an unspecified reason.Patient post operatively is doing great.The explanted devices will not return for analysis as no representative was present at the time of event.No additional information is available at this time.
Additional Manufacturer Narrative
The devices sc-2366-70 sn (b)(6), sc-2366-70 sn (b)(6) and sc-2366-70 1004377 were not returned to boston scientific for analysis and the complaint as reported was not able to be confirmed.A review of the device history record (dhr) confirmed that the devices met specification prior to shipping.No manufacturing deviations were noted that could have contributed to the event reported.Record review revealed no additional information related to the complaint.Therefore, in the absence of devices return and analysis the likely root cause could not be established.Block b3: approximated based on the date the manufacturer became aware of the event additional suspect medical device components involved in the event: model number/catalog number: sc-2366-70, serial number: (b)(6), batch/lot number: 16536641, model/catalog description: linear 3-6 lead 70 cm, unique identifier (udi) #: (b)(4).Model number/catalog number: sc-2366-70 serial number: 1004377 batch/lot number: 16536641 model/catalog description: linear 3-6 lead 70 cm unique identifier (udi) #: (01)08714729789567(17)151120(10)16536641(21)1004377.

• Brand Name: LINEAR? 3-6
• 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; 25155 rye canyon loop; valencia CA 91355
• Manufacturer Contact: erik sherburne ; 25155 rye canyon loop; valencia, CA 91355 ; 7632920920
• MDR Report Key: 24671329
• Report Number: 3006630150-2026-01742
• Device Sequence Number: 13299168
• Product Code: LGW
• Combination Product (Y/N): N
• Initial Reporter State: CO
• Initial Reporter Country: US
• PMA/510(K) Number: P030017
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2014
• Device Explanted Year: 2026
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 06/08/2026

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: 11/20/2015
• Device Model Number: SC-2366-70
• Device Catalogue Number: SC-2366-70
• Device Lot Number: 16536641
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 02/25/2026
• Supplement Date Received by Manufacturer: 04/22/2026; 05/29/2026
• Initial Report FDA Received Date: 03/23/2026
• Supplement Report FDA Received Date: 05/18/2026; 06/08/2026
• Date Device Manufactured: 11/20/2013
• 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: 42 YR
• Patient Sex: Male