FDA Adverse Event Injury Summary report: N

EON MINI

MDR report key: 3141917 · Received May 28, 2013

Report

Report Number
1627487-2013-03718
Event Type
Injury
Date Received
May 28, 2013
Date of Event
May 3, 2013
Report Date
May 3, 2013
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 Location
SC, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THIS IPG SERIAL NUMBER WAS INCLUDED IN A FIELD ADVISORY AND A FIELD CORRECTION. SJM HAS LIMITED INFO RELATED TO THE PT'S MEDICAL HISTORY AND IS UNABLE TO FORM AN OPINION AS TO THE RELEVANCY OF THE PT'S HISTORY TO THE EVENT REPORTED. SJM DEFERS TO THE PT'S PHYSICIAN REGARDING MEDICAL HISTORY.

Description of Event or Problem · 1

DEVICE 1 OF 2. REFERENCE MFR REPORT: 1627487-2013-03719. THE PT REPORTED EXPERIENCING HER SCS IPG POCKET SITE BECOMING HOT WHILE CHARGING. SUBSEQUENTLY, THE PT HAD TO TURN THE IPG OFF. THE PT IS CONSIDERING HAVING HER SCS SYSTEM EXPLANTED; HOWEVER, SHE AGREED TO THE CHARGER SWAP PROGRAM. FOLLOW-UP FROM (B)(6) 2013, IDENTIFIED THE PT STATED HER SCS IPG IS MOVING AND CAUSING PAIN AT HER POCKET SITE. THE PT HAS DECIDED TO MOVE FORWARD WITH AN EXPLANT OF THE SCS SYSTEM AND IS CONSULTING WITH HER PHYSICIAN. ON 08/01/2012 ST. JUDE MEDICAL, NEUROMODULATION DIVISION, SENT FIELD ACTION LETTERS TO PTS RELATED TO HEATING WHILE CHARGING AND RAISED AWARENESS OF THIS ISSUE TO PTS. 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
233379 EON MINI SCS IPG LGW ST. JUDE MEDICAL - NEUROMODULATION 3788 3450362

Patients

Seq Age Sex Outcome Treatment
1 71 YR Required Intervention SCS ANCHOR: MODEL 1194 (2)| IMPLANT DATE:| SCS LEAD: MODEL 3228| IMPLANT DATE: