FDA Adverse Event Injury Summary report: N

EON MINI

MDR report key: 3032294 · Received March 29, 2013

Report

Report Number
1627487-2013-01367
Event Type
Injury
Date Received
March 29, 2013
Date of Event
March 7, 2013
Report Date
March 7, 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

ADD'L # 1627487-07262012-002-R. THIS IPG SERIAL NUMBER WAS INCLUDED IN A FIELD ADVISORY AND A FIELD CORRECTION. SJM HAS LIMITED INFO 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. REF MFR REPORT: 1627487-2013-1368. IT WAS REPORTED THE PT WAS EXPERIENCING A HEATING SENSATION AT HIS IPG SITE WHILE CHARING. A NEW LE CHARGER WAS SENT TO THE PT TO ADDRESS THE ISSUE. F/U INFO IDENTIFIED THE REPLACEMENT CHARGER IS FUNCTIONING BUT THE PT IS NOT SURE IF THE POCKET IS GETTING HOT BECAUSE THE IPG IS MAKING IT SORE OR THE CHARGER. THE PT IS PENDING F/U WITH AN SJM REP. 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
130105 EON MINI SCS IPG LGW ST JUDE MEDICAL - NEUROMODULATION 3788 3290658

Patients

Seq Age Sex Outcome Treatment
1 83 YR Required Intervention IMPLANT DATE:| SCS LEAD: MODEL 3186 (2)