FDA Adverse Event Injury Summary report: N

EON MINI

MDR report key: 3231591 · Received July 12, 2013

Report

Report Number
1627487-2013-03971
Event Type
Injury
Date Received
July 12, 2013
Date of Event
June 19, 2013
Report Date
June 19, 2013
Manufacturer
ST. JUDE MEDICAL - NEUROMODULATION
Product Code
LGW
PMA / PMN Number
P010032
Removal / Correction Number
1627487-07262012-001-C
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THIS IPG SERIAL NUMBER WAS INCLUDED IN A FIELD CORRECTION. 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.

Description of Event or Problem · 1

DEVICE 1 OF 2. REFERENCE MFR. REPORT: 1627487-2013-03972. IT WAS REPORTED THE PATIENT EXPERIENCED BURNS AT HER SCS IPG POCKET SITE IN ADDITION TO RECHARGE ISSUES AND THE SCS IPG NOT TURNING ON AT TIMES. SUBSEQUENTLY, THE PATIENT IS TO HAVE HER SCS SYSTEM EXPLANTED. ADDITIONALLY, AT THIS TIME, IT IS UNKNOWN WHETHER OR NOT THE PATIENT'S CHARGING SYSTEM IS RELATED TO THE BURN ISSUE; THEREFORE, THE CHARGING SYSTEM IS BEING REPORTED AS DEVICE 2. ON 08/01/2012 ST. JUDE MEDICAL, NEUROMODULATION DIVISION, SENT FIELD ACTION LETTERS TO PATIENTS RELATED TO HEATING WHILE CHARGING AND RAISED AWARENESS OF THIS ISSUE TO PATIENTS. AN INCREASE IN PRIOR NON-REPORTED HEATING WHILE CHARGING EVENTS AND OTHER NON-REPORTED EVENTS WAS EXPECTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
323800 EON MINI SCS IPG LGW ST. JUDE MEDICAL - NEUROMODULATION 3788 3615808

Patients

Seq Age Sex Outcome Treatment
1 64 YR Other IMPLANT DATE:| SCS LEAD, MODEL 3214