LAMITRODE S8
Report
- Report Number
- 1627487-2014-03488
- Event Type
- Injury
- Date Received
- July 18, 2014
- Date of Event
- June 23, 2014
- Report Date
- June 23, 2014
- Manufacturer
- ST. JUDE MEDICAL - NEUROMODULATION
- Product Code
- GZB
- PMA / PMN Number
- P010032
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
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 2 OF 2 - REFERENCE MFR. REPORT: 1627487-2014-03487 IT WAS REPORTED THE PATIENT EXPERIENCED INCREASED RECHARGE BURDEN AND LEAD MIGRATION. AN SJM REPRESENTATIVE WAS UNABLE TO RESOLVE THE ISSUES WITH REPROGRAMMING. IT WAS ALSO REPORTED THE SCS IPG IS NOW NON-FUNCTIONAL DUE TO BATTERY DEPLETION AND THE PATIENT IS EXPERIENCING PAIN AT HER SCS IPG POCKET SITE. ON (B)(6) 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. DUE TO THE NATURE OF LITIGATION, THESE ALLEGATIONS CANNOT BE CONFIRMED OR REJECTED. 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.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 421035 | LAMITRODE S8 | SCS LEAD | GZB | ST. JUDE MEDICAL - NEUROMODULATION | 3286 | 3363915 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 34 YR | Other | IMPLANT DATE| SCS EXTENSION: MODEL 3382 |