FDA Adverse Event Injury Summary report: N

ACTIVA

MDR report key: 4433700 · Received January 20, 2015

Report

Report Number
3004209178-2015-00942
Event Type
Injury
Date Received
January 20, 2015
Report Date
December 30, 2014
Manufacturer
MEDTRONIC MED REL MEDTRONIC PUERTO RICO
Product Code
MHY
PMA / PMN Number
P960009
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

CONCOMITANT PRODUCTS: PRODUCT ID 37602, SERIAL # (B)(4), IMPLANTED: (B)(6) 2013, PRODUCT TYPE IMPLANTABLE NEUROSTIMULATOR; PRODUCT ID 3389S-40, LOT # V091844, IMPLANTED: (B)(6) 2008, PRODUCT TYPE LEAD; PRODUCT ID 7482A51, SERIAL # (B)(4), IMPLANTED: (B)(6) 2008, PRODUCT TYPE EXTENSION; PRODUCT ID 7482A51, SERIAL # (B)(4), IMPLANTED: (B)(6) 2008, PRODUCT TYPE EXTENSION; PRODUCT ID 3389S-40, LOT # V032588, IMPLANTED: (B)(6) 2008, PRODUCT TYPE LEAD; PRODUCT ID 7438, SERIAL # (B)(4), IMPLANTED: (B)(6) 2008, PRODUCT TYPE PROGRAMMER, PATIENT. (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT HAD BEEN ADMITTED TO THE HOSPITAL FOR FREQUENT FALLS. IT HAD STARTED ON SUNDAY PRIOR TO THE DATE OF THIS REPORT AND THE PATIENT HAD FALLEN THREE TIMES ON THAT DAY. THE PATIENT¿S BEHAVIORS WERE NOT LIKE THEY USED TO BE, THE PATIENT WAS HALLUCINATING, AGITATED AND COMBATIVE. THEY WANTED A MANUFACTURING REPRESENTATIVE TO COME ASSESS THE IMPLANTABLE NEUROSTIMULATOR (INS). THE PATIENT HAD PARKINSON¿S DISEASE. NO OUTCOME WAS PROVIDED. FURTHER FOLLOW-UP IS BEING CONDUCTED TO OBTAIN THIS INFORMATION. IF ADDITIONAL INFORMATION IS RECEIVED A SUPPLEMENTAL REPORT WILL BE SUBMITTED. REFERENCE MANUFACTURER¿S REPORT NUMBER: 3004209178-2015-00939.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
46786 ACTIVA STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR MHY MEDTRONIC MED REL MEDTRONIC PUERTO RICO 37602

Patients

Seq Age Sex Outcome Treatment
1 00068 YR Hospitalization