FDA Adverse Event Malfunction Summary report: N

ACTIVA

MDR report key: 2951351 · Received February 9, 2013

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

Additional Manufacturer Narrative · 1

(B)(4).

Additional Manufacturer Narrative · 1

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).

Description of Event or Problem · 1

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