FDA Adverse Event Malfunction Summary report: N

ACTIVA

MDR report key: 5051430 · Received September 2, 2015

Report

Report Number
3004209178-2015-17188
Event Type
Malfunction
Date Received
September 2, 2015
Report Date
August 11, 2015
Manufacturer
MEDTRONIC PUERTO RICO OPERATIONS CO.
Product Code
MRU
PMA / PMN Number
H020007
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) 2014, PRODUCT TYPE: IMPLANTABLE NEUROSTIMULATOR. PRODUCT ID: 3387-40, LOT# V001236, IMPLANTED: (B)(6) 2006, PRODUCT TYPE: LEAD. PRODUCT ID: 748251, SERIAL# (B)(4), IMPLANTED: (B)(6) 2006, PRODUCT TYPE: EXTENSION. PRODUCT ID: 748251, SERIAL# (B)(4), IMPLANTED: (B)(6) 2006, PRODUCT TYPE: EXTENSION. PRODUCT ID: 3387-40, LOT# J0337370V, IMPLANTED: (B)(6) 2006, PRODUCT TYPE: LEAD. PRODUCT ID: 37603, SERIAL# (B)(4), IMPLANTED: (B)(6) 2014, PRODUCT TYPE: IMPLANTABLE NEUROSTIMULATOR. (B)(4)

Description of Event or Problem · 1

INFORMATION WAS RECEIVED FROM THE PATIENT THAT REPORTED THE PATIENT'S NECK PAIN SUDDENLY RESURFACED IN MAY 2015 AFTER BEING ALLEVIATED FOR 8 YEARS. IN ADDITION, THE PATIENT HAD SEVERE MEMORY ISSUES TO THE POINT WHERE SHE WOULD WALK INTO A STORE AND WOULD NOT REMEMBER WHY SHE WENT IN. SHE HAD BEEN LOSING THINGS IN HER HOUSE BECAUSE SHE COULDN'T REMEMBER WHERE SHE PUT THEM. THE MEMORY ISSUES WERE GRADUAL STARTING IN (B)(6) 2015. THE PATIENT WAS IMPLANTED FOR DYSTONIA AND MOVEMENT DISORDERS. FURTHER FOLLOW-UP IS BEING CONDUCTED TO DETERMINE WHAT STEPS WERE TAKEN TO RESOLVE THE NECK PAIN AND MEMORY LOSS AND HAD IT BEEN RESOLVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
581853 ACTIVA IMPLANTED SUBCORTICAL ELECTRICAL STIMULATOR (MOTOR DISORDERS) MRU MEDTRONIC PUERTO RICO OPERATIONS CO. 37603

Patients

Seq Age Sex Outcome Treatment
1 00066 YR