MAUDE Adverse Event Report: ST. JUDE MED - NEUROMODULATION EON; SCS IPG

Model Number 3716

Device Problems Pocket Stimulation (1463); Low impedance (2285)

Patient Problem Inadequate Pain Relief (2388)

Event Date 07/21/2014

Event Type  Injury  

Event Description

Device 1 of 2.Reference mfr.Report: 1627487-2014-21587.It was reported the patient ((b)(6)) experienced loss of stimulation.Diagnostics revealed multiple low impedance values.The patient also stated experiencing pocket stimulation during programming.Consult with the physician is pending.

Manufacturer Narrative

Sjm has limited information related to the patient's medical history and is unable to form an opinion as to the relevancy of the patient's history to the event reported.Sjm defers to the patient's physician regarding medical history.

• Brand Name: EON
• Type of Device: SCS IPG
• Manufacturer (Section D): ST. JUDE MED - NEUROMODULATION; plano TX
• Manufacturer Contact: palka sharma ; 6901 preston rd.; plano, TX 75024 ; 9725264823
• MDR Report Key: 4092178
• MDR Text Key: 4831662
• Report Number: 1627487-2014-21586
• Device Sequence Number: 1
• Product Code: GZB
• Combination Product (y/n): N
• Reporter Country Code: AS
• PMA/PMN Number: P010032
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Foreign,Company Representative
• Reporter Occupation: Not Applicable
• Type of Report: Initial
• Report Date: 08/11/2014

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 Expiration Date: 12/01/2009
• Device Model Number: 3716
• Device Lot Number: 113373
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Initial Date Manufacturer Received: 08/11/2014
• Initial Date FDA Received: 09/03/2014
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 12/01/2007
• 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
• Patient Outcome(s): Other