ACTIVA
Report
- Report Number
- 3004209178-2013-11866
- Event Type
- Injury
- Date Received
- July 16, 2013
- Date of Event
- May 6, 2013
- Report Date
- June 21, 2013
- Manufacturer
- MEDTRONIC MED REL MEDTRONIC PUERTO RICO
- Product Code
- MHY
- PMA / PMN Number
- P960009
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- WA, US
- Reporter Occupation
- HEALTH PROFESSIONAL
Narratives
CONCOMITANT PRODUCTS: PRODUCT ID 37602, SERIAL # (B)(4), IMPLANTED: (B)(6) 2011, PRODUCT TYPE IMPLANTABLE NEUROSTIMULATOR; PRODUCT ID 37642, SERIAL # (B)(4), PRODUCT TYPE PROGRAMMER, PATIENT; PRODUCT ID 3389S-40, LOT # V324755, IMPLANTED: (B)(6) 2009, PRODUCT TYPE LEAD; PRODUCT ID 7482A51, SERIAL # (B)(4), IMPLANTED: (B)(6) 2009, PRODUCT TYPE EXTENSION; PRODUCT ID 3389S-40, LOT # V323742, IMPLANTED: (B)(6) 2009, PRODUCT TYPE LEAD; PRODUCT ID 7482A51, SERIAL # (B)(4), IMPLANTED: (B)(6) 2009, PRODUCT TYPE EXTENSION. (B)(4).
IT WAS REPORTED THAT THE PATIENT FELL AROUND (B)(6) AND FRACTURED HER ARM, ALSO DAMAGING HER RADIAL NERVE. IT WAS NOTED THAT WHILE THE DBS DID HELP WITH THE PATIENT'S PARKINSON¿S SYMPTOMS, SHE STILL EXPERIENCED SOME RIGIDITY AND TONE SYMPTOMS AND DIFFICULTY WALKING. IN THE CASE OF THE FALL, THE PATIENT FROZE AND WAS UNABLE TO CATCH HERSELF BEFORE FALLING. IT WAS NOTED THAT THE FALL WAS NOT RELATED TO THE PATIENT¿S IMPLANT. ADDITIONAL INFORMATION HAS BEEN REQUESTED, BUT WAS NOT AVAILABLE AS OF THE DATE OF THIS REPORT. SEE ALSO MFR. REP. # 3004209178-2013-11864
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 328968 | ACTIVA | STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR | MHY | MEDTRONIC MED REL MEDTRONIC PUERTO RICO | 37602 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 00062 YR | Required Intervention |