FDA Adverse Event Malfunction Summary report: N

SOLETRA

MDR report key: 2842899 · Received November 21, 2012

Report

Report Number
3004209178-2012-10676
Event Type
Malfunction
Date Received
November 21, 2012
Report Date
October 25, 2012
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
VA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

PRODUCT ID, 748251 LOT# SERIAL# (B)(4), IMPLANTED: 2004 (B)(6), PRODUCT TYPE EXTENSION PRODUCT ID, 748251 LOT# SERIAL# (B)(4), IMPLANTED: 2004 (B)(6), PRODUCT TYPE EXTENSION PRODUCT ID, 7438 LOT# SERIAL# (B)(4), IMPLANTED: 2004 (B)(6), PRODUCT TYPE PROGRAMMER, PATIENT PRODUCT ID, 3387-40 LOT# J0424862V, IMPLANTED: 2004 (B)(6), PRODUCT TYPE LEAD PRODUCT ID, 3387-40 LOT# J0406018V, IMPLANTED: 2004 (B)(6), PRODUCT TYPE LEAD. (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT HAD A LOSS OF THERAPEUTIC EFFECT. THE PATIENT HAD TREMORS IN HIS HANDS THAT BEGAN THE DAY PRIOR TO THE REPORT. THE PATIENT STATED, HE WENT TO A STORE ON (B)(6) 2012 AND WENT THROUGH A SECURITY GATE THAT "SOMETIMES" SHUT HIS STIMULATION OFF. IT WAS ALSO REPORTED THAT THE PATIENT'S PROGRAMMER WAS "NOT WORKING." THE PATIENT "JUST" CHANGED THE BATTERY AND A GREEN LIGHT WAS ON. THE PATIENT TRIED TURNING STIMULATION ON AND ONLY THE GREEN LIGHT CAME ON. ADDITIONAL INFORMATION WAS REQUESTED, BUT WAS NOT AVAILABLE AS OF THE DATE OF THIS REPORT.

Description of Event or Problem · 1

FOLLOW UP REPORTED THE PATIENT HAD RECEIVED ASSISTANCE FROM THEIR DOCTOR OR REPRESENTATIVE AND THEIR CONCERNS WERE RESOLVED. IT WAS NOTED THERE WAS AN APPOINTMENT ON (B)(6) 2012.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SOLETRA STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR MHY MEDTRONIC MED REL MEDTRONIC PUERTO RICO 7426

Patients

Seq Age Sex Outcome Treatment
1