MAUDE Adverse Event Report: Abbott Medical Quattrode Lead Wide Spaced, 60 cm; SCS Lead

Model Number	3166
Medical Device Problem Code	Migration (4003)
Health Effect - Clinical Code	Inadequate Pain Relief (2388)
Date of Event	08/24/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that the patient experienced ineffective therapy.X-ray imaging revealed migration of the lead.As a result, surgical intervention was undertaken on (b)(6) 2026 wherein the lead was repositioned to address the issue.
Additional Manufacturer Narrative
Date of event is estimated.

• Brand Name: Quattrode Lead Wide Spaced, 60 cm
• Common Device Name: SCS Lead
• Manufacturer (Section D): Abbott Medical; 6901 preston rd; plano TX 75024
• Manufacturer (Section G): Abbott Medical; 6901 preston rd; plano TX 75024
• Manufacturer Contact: sara speyerer ; 6901 preston road; plano, TX 75024 ; +1(972)309-8000
• MDR Report Key: 50849947
• Report Number: 1627487-2026-10198
• Device Sequence Number: 15959082
• Product Code: LGW
• UDI-Device Identifier: 05414734401661
• UDI-Public: (01)05414734401661(10)T00006353(17)260813
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2025
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 09/21/2026

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: Health Professional
• Device Expiration Date: 08/13/2026
• Device Model Number: 3166
• Device Catalogue Number: 3166
• Device Lot Number: T00006353
• 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: 08/24/2026
• Initial Report FDA Received Date: 09/22/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 08/13/2024
• 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
• Concomitant Medical Products and Therapy/Usage Dates: SCS Extension (x2); SCS IPG; SCS Lead (x3)
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Female
• Patient Weight: 150 LB