FDA Adverse Event Injury Summary report: N

EON

MDR report key: 3221761 · Received July 9, 2013

Report

Report Number
1627487-2013-06574
Event Type
Injury
Date Received
July 9, 2013
Date of Event
June 12, 2013
Report Date
June 12, 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 MODEL WAS INCLUDED IN 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: 1627487-2013-06575. IT WAS REPORTED THE PT EXPERIENCED HEATING WHILE CHARGING HER IPG. AN SJM REP CONTACTED THE PT AND SHE STATED THAT SHE HAD NOT FOLLOWED HER NORMAL CHARGING SCHEDULE AND HAD TO CHARGE FOR A LONGER PERIOD OF TIME WHEN SHE EXPERIENCED THE HEATING. THE PT WILL TRY CHARGING HER IPG FOR SHORTER INTERVALS. THE REP ADVISED THE PT TO CALL SJM IF THE HEATING PERSISTS. ON 08/01/2012, ST. JUDE MEDICAL, NEUROMODULATION DIVISION, SENT FIELD ACTION LETTERS TO PT RELATED TO HEATING WHILE CHARGING AND RAISED AWARENESS OF THIS ISSUE TO PTS. AN INCREASE IN PRIOR NON-REPORTED HEARING WHILE CHARGING EVENTS AND OTHER NON-REPORTED EVENTS WAS EXPECTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
313582 EON SCS IPG LGW ST. JUDE MEDICAL - NEUROMODULATION 3716 UNK

Patients

Seq Age Sex Outcome Treatment
1 63 YR Other SCS LEAD: MODEL 3186| SCS ANCHOR: MODEL 1194| SCS LEAD: MODEL 3186| IMPLANT DATE:| IMPLANT DATE:| IMPLANT DATE:| IMPLANT DATE:| SCS ANCHOR: MODEL 1194