MAUDE Adverse Event Report: ABBOTT MEDICAL KIT IMPLANTABLE SLIM TIP LEAD, 50CM; DRG LEAD

Model Number MN20450-50A

Device Problem High impedance (1291)

Patient Problems Failure of Implant (1924); Inadequate Pain Relief (2388)

Event Date 03/12/2024

Event Type  Injury  

Manufacturer Narrative

Additional components potentially involved in the event include: common device name: drg lead, model: mn20450-50a , udi:(b)(6), serial: (b)(6), batch:9171081.

Event Description

Related manufacturer reference number: 1627487-2024-07938 it was reported that the patient experienced i(b)(4)neffective therapy due to high impedances on two of the leads.Reprogramming was unable to resolve the issue.Investigation was unable to determine which two leads had high impedances.

Event Description

Additional information was received indicating surgical intervention was undertaken wherein the impeded leads were explanted and replaced to resolve the issue.

• Brand Name: KIT IMPLANTABLE SLIM TIP LEAD, 50CM
• Type of Device: DRG 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: heidi syndergaard ; 6901 preston road; plano, TX 75024 ; 9723098000
• MDR Report Key: 19041828
• MDR Text Key: 339433867
• Report Number: 1627487-2024-07937
• Device Sequence Number: 1
• Product Code: PMP
• UDI-Device Identifier: 05415067027368
• UDI-Public: (01)05415067027368(10)9171081(17)250813
• Combination Product (y/n): N
• Reporter Country Code: BR
• PMA/PMN Number: P150004
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Foreign,Health Professional,Company Representative
• Reporter Occupation: Physician
• Type of Report: Initial
• Report Date: 04/04/2024

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
• Device Operator: Health Professional
• Device Model Number: MN20450-50A
• Device Lot Number: 9171081
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Initial Date Manufacturer Received: 03/12/2024
• Initial Date FDA Received: 04/04/2024
• Date Device Manufactured: 08/14/2023
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Treatment: DRG LEAD
• Patient Outcome(s): Other