FDA Adverse Event Injury Summary report: N

RESTORE

MDR report key: 3673434 · Received March 11, 2014

Report

Report Number
3004209178-2014-04266
Event Type
Injury
Date Received
March 11, 2014
Report Date
February 20, 2014
Manufacturer
MEDTRONIC MED REL MEDTRONIC PUERTO RICO
Product Code
LGW
PMA / PMN Number
P840001
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

PRODUCT ID 377860, LOT# V011437, IMPLANTED: 2006 (B)(6); PRODUCT TYPE LEAD PRODUCT ID 37742, SERIAL# (B)(4), IMPLANTED: 2006 (B)(6); PRODUCT TYPE PROGRAMMER, PATIENT PRODUCT ID 37752, SERIAL# (B)(4), IMPLANTED: 2006 (B)(6); PRODUCT TYPE RECHARGER PRODUCT ID 377860, LOT# V011437, IMPLANTED: 2006 (B)(6); PRODUCT TYPE LEAD PRODUCT ID 37743, SERIAL# (B)(4); PRODUCT TYPE PROGRAMMER, PATIENT PRODUCT ID 3708120, SERIAL# (B)(4), IMPLANTED: 2009 (B)(6); PRODUCT TYPE EXTENSION PRODUCT ID 3777-45, SERIAL# (B)(4), IMPLANTED: 2009 (B)(6); PRODUCT TYPE LEAD PRODUCT ID 3708120, SERIAL# (B)(4), IMPLANTED: 2009 (B)(6); PRODUCT TYPE EXTENSION PRODUCT ID 3778-45, SERIAL# (B)(4), IMPLANTED: 2009 (B)(6); PRODUCT TYPE LEAD PRODUCT ID 37752, SERIAL# (B)(4); PRODUCT TYPE RECHARGER PRODUCT ID 37712, SERIAL# (B)(4), IMPLANTED: 2009 (B)(6); PRODUCT TYPE IMPLANTABLE NEUROSTIMULATOR. (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED, THE PATIENTS IMPLANTABLE NEUROSTIMULATOR WAS IN OVERDISCHARGE. ADDITIONAL INFORMATION RECEIVED REPORTED THE PATIENT WAS PROBABLY GOING TO GET THE SYSTEM REPLACED WITH ANOTHER DEVICE SINCE HE HAS MS.

Description of Event or Problem · 1

ADDITIONAL INFORMATION RECEIVED REPORTED THE PATIENT HAD NOT BEEN SCHEDULE AND THEY WERE NOT SURE WHEN THE REVISION WOULD TAKE PLACE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
145836 RESTORE STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF LGW MEDTRONIC MED REL MEDTRONIC PUERTO RICO 37711

Patients

Seq Age Sex Outcome Treatment
1 00059 YR Required Intervention