MAUDE Adverse Event Report: ST. JUDE MEDICAL - NEUROMODULATION 50CM TRIAL LEAD KIT, SLIM TIP; DRG LEAD

Model Number	MN10350-50A
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Pain (1994)
Date of Event	02/11/2019
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Patient¿s dob is unknown at this time.The results/method and conclusion codes along with investigation results will be provided in the final report.
Event or Problem Description
Device 2 of 2: reference mfr.Report: 1627487-2019-02729.It was reported the patient was to undergo a drg trial implant procedure on (b)(6) 2019 and the physician implanted two leads.While the patient was in recovery, the patient reported the pain behind the leg was worse when laying down.To address the issue, the physician explanted the two trial leads.
Event or Problem Description
Device 2 of 2.Reference mfr.Report: 1627487-2019-02729.Follow up information identified the patient had a failed trial, and the leads were explanted, as previously reported.Further information was requested but not received.
Event or Problem Description
Device 2 of 2.Reference mfr.Report: 1627487-2019-02729.

• Brand Name: 50CM TRIAL LEAD KIT, SLIM TIP
• Common Device Name: DRG LEAD
• Manufacturer (Section D): ST. JUDE MEDICAL - NEUROMODULATION; 6901 preston rd; plano TX 75024
• MDR Report Key: 8379506
• Report Number: 1627487-2019-02730
• Device Sequence Number: 19589592
• Product Code: PMP
• UDI-Device Identifier: 05415067025517
• UDI-Public: 05415067025517
• Combination Product (Y/N): N
• Initial Reporter State: OH
• Initial Reporter Country: US
• PMA/510(K) Number: P150004
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2019
• Device Explanted Year: 2019
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 05/10/2019

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: 06/22/2019
• Device Model Number: MN10350-50A
• Device Catalogue Number: MN10350-50A
• Device Lot Number: AB2360
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Initial Date Received by Manufacturer: 02/11/2019
• Supplement Date Received by Manufacturer: 05/07/2019; 05/10/2019
• Initial Report FDA Received Date: 02/28/2019
• Supplement Report FDA Received Date: 05/07/2019; 05/10/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: MODEL MN10350-50A, DRG LEAD
• Outcome Attributed to Adverse Event: Other