SOLETRA
Report
- Report Number
- 3004209178-2013-12074
- Event Type
- Injury
- Date Received
- July 22, 2013
- Report Date
- June 25, 2013
- Manufacturer
- MEDTRONIC MED REL MEDTRONIC PUERTO RICO
- Product Code
- MHY
- PMA / PMN Number
- H020007
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AR, US
- Reporter Occupation
- OTHER
Narratives
CONCOMITANT MEDICAL PRODUCTS: PRODUCT ID 7426, SERIAL# (B)(4), IMPLANTED: (B)(6) 2006. PRODUCT TYPE: IMPLANTABLE NEUROSTIMULATOR: PRODUCT ID 7482, SERIAL# (B)(4), IMPLANTED: (B)(6) 2006. PRODUCT TYPE: EXTENSION: PRODUCT ID 3387, LOT# V005849, IMPLANTED: (B)(6) 2006. PRODUCT TYPE: LEAD: PRODUCT ID 3387, LOT# V005849, IMPLANTED: (B)(6) 2006. PRODUCT TYPE: LEAD: PRODUCT ID 7482, SERIAL# (B)(4), IMPLANTED: (B)(6) 2006. PRODUCT TYPE: EXTENSION: PRODUCT ID 7438, SERIAL# (B)(4), IMPLANTED: (B)(6) 2006. PRODUCT TYPE: PROGRAMMER, PATIENT. (B)(4).
(B)(4).
ADDITIONAL INFORMATION RECEIVED REPORTED ALL HER COMPONENTS WERE TAKEN OUT BUT ONE WAS LEFT IN. THE PATIENT WAS TOLD IT WAS TOO DANGEROUS TO REMOVE THE COMPONENT BUT SHE DID NOT KNOW WHICH ONE. PER THE MANUFACTURER¿S DEVICE REGISTRY THE PATIENT¿S LEADS WERE NOT REMOVED.
IT WAS REPORTED THE PATIENT¿S DEVICE SYSTEM WAS REMOVED SOMETIME IN 2006 OR EARLY 2007 BECAUSE IT WAS NOT WORKING SO HER PHYSICIAN DECIDED ON REMOVAL. IT WAS NOTED THE PATIENT CURRENTLY STILL HAD A LOT OF SHAKING AND TREMORS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 339642 | SOLETRA | STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR | MHY | MEDTRONIC MED REL MEDTRONIC PUERTO RICO | 7426 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 00052 YR | Required Intervention |