FDA Adverse Event Malfunction Summary report: N

INTERSTIM II

MDR report key: 2842991 · Received November 21, 2012

Report

Report Number
3004209178-2012-10699
Event Type
Malfunction
Date Received
November 21, 2012
Report Date
October 26, 2012
Manufacturer
MEDTRONIC MED REL MEDTRONIC PUERTO RICO
Product Code
EZW
PMA / PMN Number
P970004
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

PRODUCT ID, 3093-33 LOT# V241655, IMPLANTED: 2009 (B)(6), PRODUCT TYPE LEAD PRODUCT ID, 3093-33 LOT# V241655, IMPLANTED: 2009 (B)(6), PRODUCT TYPE LEAD PRODUCT ID, 3037 LOT# SERIAL# (B)(4) PRODUCT TYPE PROGRAMMER, PATIENT PRODUCT ID, 3037 LOT# SERIAL# (B)(4), PRODUCT TYPE PROGRAMMER, PATIENT PRODUCT ID, 3058 LOT# SERIAL# (B)(4), IMPLANTED: 2009 (B)(6), PRODUCT TYPE IMPLANTABLE NEUROSTIMULATOR. (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED, THE PATIENT EXPERIENCED A SHOCKING SENSATION WHENEVER SHE WENT THROUGH WALMART, AUTO ZONE, OR TOYS R US SECURITY GATES. THE PATIENT STARTED EXPERIENCING THE SHOCKING 3 YEARS AGO. THE PATIENT ALSO NOTICED ABOUT A YEAR AGO SHE STARTED GETTING SHOCKED WHEN A WAND WAS USED; IT WAS NOTED THIS HAD NOT HAPPENED IN THE PAST. IT WAS ALSO REPORTED THE PATIENT'S PROGRAMMING WAS CHANGED BUT SHE WAS UNABLE TO CONFIRM IF IT ACTUALLY CHANGED. THE PATIENT WAS TOLD BY HER PROGRAMMER HER SETTINGS WERE UNUSUAL. IT WAS ALSO REPORTED THE PATIENT STARTED GETTING SHOCKS WHEN LAYING DOWN WRONG 3 DAYS PRIOR TO THIS REPORT. THE PATIENT WAS ALSO "AWARE"OF HER DEVICE "ALL THE TIME." ADDITIONAL INFORMATION HAS BEEN REQUESTED BUT WAS NOT AVAILABLE AS OF THE DATE OF THIS REPORT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 INTERSTIM II STIMULATOR, ELECTRICAL, IMPLANTABLE, FOR INCONTINENCE EZW MEDTRONIC MED REL MEDTRONIC PUERTO RICO 3058

Patients

Seq Age Sex Outcome Treatment
1