FDA Adverse Event Malfunction Summary report: N

ACTIVA

MDR report key: 4375684 · Received December 31, 2014

Report

Report Number
3004209178-2014-24740
Event Type
Malfunction
Date Received
December 31, 2014
Report Date
December 10, 2014
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
MD, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

CONCOMITANT MEDICAL PRODUCTS: PRODUCT ID: 37603, SERIAL# (B)(4), IMPLANTED: (B)(6) 2012, PRODUCT TYPE: IMPLANTABLE NEUROSTIMULATOR. PRODUCT ID: 3389S-40, LOT# V972376, IMPLANTED: (B)(6) 2012, PRODUCT TYPE: LEAD. PRODUCT ID: 37085-60, SERIAL# (B)(4), IMPLANTED: (B)(6) 2012, PRODUCT TYPE: EXTENSION. PRODUCT ID: 37642, SERIAL# (B)(4), PRODUCT TYPE: PROGRAMMER, PATIENT. PRODUCT ID: 37085-60, SERIAL# (B)(4), IMPLANTED: (B)(6) 2012, PRODUCT TYPE: EXTENSION. (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THE PATIENT FELT A ¿PRICKLY¿ FEELING TODAY WHILE THEY HAD UROPLASTY DONE WITH ELECTRODES PLACED ON THEIR ANKLE. THE PATIENT FELT THE SENSATION IN THEIR BRAIN, BUT IT COULD HAVE BEEN THEIR SCALP. THE PATIENT¿S IMPLANTABLE NEUROSTIMULATOR (INS) WAS OFF FOR THE THERAPY. IN THE PAST THE PATIENT HAD STIMULATION ON AND THEY FELT THE SAME FEELING SO THEY STARTED TO TURN STIMULATION OFF. THE PATIENT WONDERED WHY THEY FELT THE SENSATION WITH THE INS OFF. NO INTERVENTIONS OR OUTCOME WERE REPORTED REGARDING THIS EVENT. FURTHER FOLLOW-UP IS BEING CONDUCTED TO OBTAIN THIS INFORMATION. IF ADDITIONAL INFORMATION IS RECEIVED, A FOLLOW UP REPORT WILL BE SENT. REFER TO MANUFACTURER REPORT #3004209178-2014-24739.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
862109 ACTIVA STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR MHY MEDTRONIC MED REL MEDTRONIC PUERTO RICO 37603

Patients

Seq Age Sex Outcome Treatment
1