EON MINI
Report
- Report Number
- 1627487-2013-15624
- Event Type
- Injury
- Date Received
- May 9, 2013
- Date of Event
- March 27, 2013
- Report Date
- April 19, 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
- TX, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
A 1627487-05242011-002-R, 1627487-07262012-001-C. THIS IPG SERIAL NUMBER WAS INCLUDED IN FIELD ADVISORIES 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.
DEVICE 2 OF 4. REFERENCE MFR REPORT: 1627487-2013-15623. REFERENCE MFR REPORT: 1627487-2013-15625. REFERENCE MFR REPORT: 1627487-2013-15626. THE PT HAS 2 SCS SYSTEMS IMPLANTED. IT WAS REPORTED THE PT EXPERIENCED PAINFUL HEATING RELATED TO BOTH OF HER IPGS. THE PT'S IPGS WERE PREVIOUSLY EXPLANTED AFTER THE PT FELL AND LOST STIMULATION (REFERENCE MFR REPORTS: 1627487-2013-1307 AND 1627487-2013-1308). NO ADDITIONAL INFO IS AVAILABLE AT THIS TIME. 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 |
|---|---|---|---|---|---|---|---|
| 204683 | EON MINI | SCS IPG | LGW | ST. JUDE MEDICAL - NEUROMODULATION | 3788 | 2819331 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 41 YR | Required Intervention | SCS LEAD: MODEL 3214| SCS LEAD: MODEL 3219| IMPLANTED:| IMPLANTED: |