MAUDE Adverse Event Report: Abbott Medical Kit Implantable Slim Tip Lead, 90cm; Dorsal Root Ganglion Stimulator For Pain Relief

Model Number	MN10450-90A
Medical Device Problem Codes	Therapeutic or Diagnostic Output Failure (3023); No Apparent Adverse Event (3189)
Health Effect - Clinical Codes	Inadequate Pain Relief (2388); No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/09/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
Additional information indicates the patient experienced new pain and not ineffective therapy; therefore, this device is no longer considered reportable.
Event or Problem Description
It was reported that the patient experienced ineffective therapy.Reprogramming is unable to resolve the issue.As a result, surgical intervention may be undertaken to address the issue.It is unknown which lead the allegation is against.
Additional Manufacturer Narrative
Additional information indicates the patient experienced new pain and not ineffective therapy; therefore, this device is no longer considered reportable.The results of the investigation are inconclusive since the device was not returned for analysis.Based on the information received, the cause of the reported incident could not be conclusively determined.
Additional Manufacturer Narrative
Date of event is estimated.Additional components potentially involved in the event include: common device name: kit implantable slim tip lead, 90cm, model: mn10450-90a, udi: (b)(4), serial: (b)(6), batch: 7034950.

• Brand Name: Kit Implantable Slim Tip Lead, 90cm
• Common Device Name: Dorsal Root Ganglion Stimulator For Pain Relief
• 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: 50128659
• Report Number: 1627487-2026-09321
• Device Sequence Number: 20243232
• Product Code: PMP
• UDI-Device Identifier: 05415067027160
• UDI-Public: (01)05415067027160(10)6607553(17)200828
• Combination Product (Y/N): N
• Initial Reporter State: WV
• Initial Reporter Country: US
• PMA/510(K) Number: P150004
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2020
• Device Explanted Year: 2026
• 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,Followup
• Report Date (Section B): 09/30/2026

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: 08/28/2020
• Device Model Number: MN10450-90A
• Device Catalogue Number: MN10450-90A
• Device Lot Number: 6607553
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/09/2026
• Supplement Date Received by Manufacturer: 09/15/2026; 09/25/2026
• Initial Report FDA Received Date: 08/04/2026
• Supplement Report FDA Received Date: 09/24/2026; 09/30/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 08/29/2018
• 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
• Concomitant Medical Products and Therapy/Usage Dates: DRG IPG; DRG LEAD
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Female
• Patient Weight: 180 LB