ACTIVA
Report
- Report Number
- 3004209178-2013-01506
- Event Type
- Malfunction
- Date Received
- February 9, 2013
- Date of Event
- November 16, 2012
- Report Date
- January 21, 2013
- 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
- OH, US
- Reporter Occupation
- OTHER
Narratives
(B)(4).
CONCOMITANT MEDICAL PRODUCTS: PRODUCT ID 748251, SERIAL# (B)(4), IMPLANTED: (B)(6) 2005. PRODUCT TYPE: EXTENSION: PRODUCT ID 748251, SERIAL# (B)(4), IMPLANTED: (B)(6) 2006. PRODUCT TYPE: EXTENSION: PRODUCT ID 3389S-40, LOT# V010793, IMPLANTED: (B)(6) 2006. PRODUCT TYPE: LEAD: PRODUCT ID 3387-40, LOT# J0519620V, IMPLANTED: (B)(6) 2005. PRODUCT TYPE: LEAD. (B)(4).
IT WAS REPORTED THE PATIENT HAD THEIR TEETH REMOVED IN (B)(6) 2012. IT WAS NOTED THAT THE PATIENT FELT LIKE "IT HAD DONE SOMETHING TO THEM." IT WAS UNCLEAR WHAT TYPE OF EQUIPMENT, OR OTHER ACCESSORIES THE DENTIST USED AND IF THAT AFFECTED THE PATIENT'S DEVICE. THE PATIENT'S SPEECH WAS REPORTED AS "OFF." IT WAS ALSO UNCLEAR IF THAT WAS DEVICE RELATED OR NOT. IT WAS NOTED THE "THING WAS OFF." IT WAS UNCLEAR IF THIS WAS REFERRING TO THE DEVICE OR SOMETHING ELSE. IT WAS INDICATED THE PATIENT HAD AN APPOINTMENT WITH THEIR HEALTHCARE PROVIDER IN (B)(6) 2013. ADDITIONAL INFORMATION HAS BEEN REQUESTED, A FOLLOW UP REPORT WILL BE SENT IF ADDITIONAL INFORMATION IS RECEIVED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 55978 | ACTIVA | STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR | MHY | MEDTRONIC MED REL MEDTRONIC PUERTO RICO | 37602 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 00053 YR |