SOLETRA
Report
- Report Number
- 3004209178-2015-20019
- Event Type
- Malfunction
- Date Received
- October 5, 2015
- Report Date
- September 10, 2015
- Manufacturer
- MEDTRONIC MED REL MEDTRONIC PUERTO RICO
- Product Code
- MHY
- PMA / PMN Number
- P960009
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- KY, US
- Reporter Occupation
- OTHER
Narratives
CONCOMITANT PRODUCTS: PRODUCT ID 7426, SERIAL # (B)(4), IMPLANTED: (B)(6) 2010, PRODUCT TYPE IMPLANTABLE NEUROSTIMULATOR; PRODUCT ID 3387S-40, LOT # V331504, IMPLANTED: (B)(6) 2010, PRODUCT TYPE LEAD; PRODUCT ID 7482A51, SERIAL # (B)(4), IMPLANTED: (B)(6) 2010, PRODUCT TYPE EXTENSION; PRODUCT ID 3387S-40, LOT # V285124, IMPLANTED: (B)(6) 2009, PRODUCT TYPE LEAD; PRODUCT ID 3550-05, LOT # N221537, IMPLANTED: (B)(6) 2009, PRODUCT TYPE ACCESSORY; PRODUCT ID 7482A51, SERIAL # (B)(4), IMPLANTED: (B)(6) 2009, PRODUCT TYPE EXTENSION; PRODUCT ID 3550-05, LOT # N221537, IMPLANTED: (B)(6) 2009, PRODUCT TYPE ACCESSORY. (B)(4).
INFORMATION WAS RECEIVED FROM THE PATIENT THAT REPORTED THEY DIDN¿T FEEL THE DEEP BRAIN STIMULATOR (DBS) WAS WORKING ANYMORE. THE DEVICE WAS HELPING TO CONTROL HIS TREMORS BUT NOW THEY HAD MODERATE HEAD AND NECK TREMORS. THE PATIENT WAS IMPLANTED FOR ESSENTIAL TREMOR. FURTHER FOLLOW-UP IS BEING CONDUCTED TO DETERMINE WHAT STEPS WERE TAKEN TO RESOLVE THE HEAD AND NECK TREMORS. IF ADDITIONAL INFORMATION IS RECEIVED, A FOLLOW-UP REPORT WILL BE SUBMITTED. **PLEASE SEE MANUFACTURER REPORT #3004209178-2015-20017 FOR INFORMATION ON THE PATIENT'S CONCOMITANT SYSTEM.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 659473 | SOLETRA | STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR | MHY | MEDTRONIC MED REL MEDTRONIC PUERTO RICO | 7426 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 00044 YR |