FDA Adverse Event Injury Summary report: N

EON MINI

MDR report key: 2772029 · Received October 2, 2012

Report

Report Number
1627487-2012-02406
Event Type
Injury
Date Received
October 2, 2012
Date of Event
September 10, 2012
Report Date
September 10, 2012
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
OR, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

CORRECTION: 1627487-12192011-003-R AND 1627487-07262012-002-R. THIS IPG SERIAL NUMBER WAS INCLUDED IN A FIELD CORRECTION AND FIELD ADVISORY. 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: 1627487-2012-02407. IT WAS REPORTED, THE PT EXPERIENCED A HEATING SENSATION AT HIS IPG POCKET SITE WHILE CHARGING. THE PT REPORTED, HE CHARGES EVERY 1.5 MONTHS FOR ABOUT 1.5 HOURS AT A TIME AND THE HEATING BEGINS ABOUT 30 MINUTES INTO CHARGING. HE STATED, HE PLACES THE ANTENNA PADDLE DIRECTLY ON HIS SKIN TO CHARGE. THE SJM REP ADVISED THE PT OF CHARGING PRECAUTIONS. FOLLOW-UP IDENTIFIED THE CHARGING RECOMMENDATIONS HAVE ALLEVIATED THE ISSUE ALTHOUGH THE PT NOW FINDS CHARGING TO BE MORE INCONVENIENT. ON 08/01/2012 ST. JUDE MEDICAL, NEUROMODULATION DIV, 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
1 EON MINI SCS IPG LGW ST. JUDE MEDICAL - NEUROMODULATION 3788 2881387

Patients

Seq Age Sex Outcome Treatment
1 56 YR Required Intervention SCS LEAD: MODEL 3219| IMPLANT DATE: