FDA Adverse Event Malfunction Summary report: N

ITREL 3

MDR report key: 2053609 · Received March 1, 2011

Report

Report Number
3004209178-2011-01520
Event Type
Malfunction
Date Received
March 1, 2011
Date of Event
January 1, 2011
Report Date
February 11, 2011
Manufacturer
MDT PUERTO RICO OPERATIONS CO., JUNCOS
Product Code
LGW
PMA / PMN Number
P840001
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NM, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

RECEIVED INFO THE INS WAS TURNING ITSELF OFF. SOMETIMES THE STIMULATION WOULD NOT TURN BACK ON UNTIL THE PT HAD WAITED AWHILE. SO HE NOW WAITS ABOUT 10 MINUTES AND USES THE PT PROGRAMMER TO TURN STIMULATION BACK ON AGAIN. THE INS STARTED DOING THIS ABOUT ONE MONTH AGO. PT ALSO NOW HAS STIMULATION IN HIS LEFT LEG, WHICH HE DID NOT HAVE BEFORE. ADD'L INFO HAS BEEN REQUESTED AND IF RECEIVED, A FOLLOW UP REPORT WILL BE SENT. REFER TO MFR REPORT # 3004209178-2011-01519 FOR ADD'L INS SYSTEM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ITREL 3 LGW MDT PUERTO RICO OPERATIONS CO., JUNCOS 7425 NA

Patients

Seq Age Sex Outcome Treatment
1 71 YR EXTENSION: MODEL 37082, LOT # NKB003180N| EXPLANTED:| IMPLANTABLE NEURO STIMULATOR: MODEL 37711,| IMPLANTED:| LEAD: MODEL 3998, LOT # V027462| EXPLANTED:| EXPLANTED:| LEAD: MODEL 3587A, LOT # L70301| LOT # NJH715924H| IMPLANTED:| IMPLANTED:| ACCESSORY: MODEL 37752, LOT # NKA028629N| PROGRAMMER: MODEL 37742, LOT # NJD055146N| EXPLANTED:| IMPLANTED:| IMPLANTED:| PROGRAMMER: MODEL 7434A, LOT # NGL022018P| EXPLANTED:| EXTENSION: MODEL 7495-51, LOT # XR0065385N