FDA Adverse Event Injury Summary report: N

EON MINI

MDR report key: 3231395 · Received July 12, 2013

Report

Report Number
1627487-2013-08350
Event Type
Injury
Date Received
July 12, 2013
Date of Event
June 19, 2013
Report Date
January 15, 2015
Manufacturer
ST. JUDE MEDICAL - NEUROMODULATION
Product Code
LGW
PMA / PMN Number
P010032
Removal / Correction Number
1627487-07262012-002-R
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
NOT APPLICABLE
Health Professional
N

Narratives

Additional Manufacturer Narrative · 1

CORRECTION NUMBER: 1627487-07262012-001-C. THIS IPG SERIAL NUMBER WAS INCLUDED IN A FIELD ADVISORIES AND 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: 1627487-2013-08351. IT WAS REPORTED THE PATIENT EXPERIENCED BURNS AT THE IPG (IMPLANTABLE PULSE GENERATOR) SITE AND BATTERY RECHARGE PROBLEMS. IT WAS STATED THE PT WAS IN THE PROCESS TO HAVE AN EXPLANT. 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
322355 EON MINI SCS IPG LGW ST. JUDE MEDICAL - NEUROMODULATION 3788 3240699

Patients

Seq Age Sex Outcome Treatment
1 50 YR Female Other IMPLANT DATE: | IMPLANT DATE: | IMPLANT DATE: | SCS EXTENSION, MODEL 3341 (2) | SCS LEAD, MODEL 3163 (2) | SCS LEAD, MODEL 3166 (2) | IMPLANT DATE:| SCS LEAD, MODEL 3166 (2)| IMPLANT DATE:| IMPLANT DATE:| SCS EXTENSION, MODEL 3341 (2)| SCS LEAD, MODEL 3163 (2)