EON MINI
Report
- Report Number
- 1627487-2013-02270
- Event Type
- Injury
- Date Received
- February 22, 2013
- Date of Event
- January 29, 2013
- Report Date
- January 30, 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
- OTHER
Narratives
CORRECTION: 1627487-05242011-002-R AND 1627487-12192011-003-R. 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.
DEVICE 1 OF 2. REFERENCE MFR REPORT # 1627487-2013-02271. IT WAS REPORTED, THE PT EXPERIENCED HEATING AT HER IPG POCKET SITE WHILE CHARGING. THE PT STATED, SHE HAD A SLIGHT BURN ON HER SKIN AFTER CHARGING FOR TWO HOURS. THE SJM REP ADVISED THE PT OF CHARGING PRECAUTIONS. FOLLOW-UP IDENTIFIED A REPLACEMENT CHARGING SYS RESOLVED THE ISSUE. 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 |
|---|---|---|---|---|---|---|---|
| 78691 | EON MINI | SCS IPG | LGW | ST. JUDE MEDICAL - NEUROMODULATION | 3788 | 3071749 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 45 YR | Required Intervention | IMPLANT DATE:| SCS LEAD: MODEL 3225 (2) |