FDA Adverse Event Injury Summary report: N

QUATTRODE

MDR report key: 3366326 · Received September 18, 2013

Report

Report Number
1627487-2013-22030
Event Type
Injury
Date Received
September 18, 2013
Date of Event
August 27, 2013
Report Date
August 27, 2013
Manufacturer
ST. JUDE MEDICAL - NEUROMODULATION
Product Code
LGW
PMA / PMN Number
K072462
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

SJM HAS LIMITED INFORMATION RELATED TO THE PATIENT'S MEDICAL HISTORY AND IS UNABLE TO FORM AN OPINION AS TO THE RELEVANCY OF THE PATIENT'S HISTORY TO THE EVENT REPORTED. SJM DEFERS TO THE PATIENT'S PHYSICIAN REGARDING MEDICAL HISTORY.

Description of Event or Problem · 1

DEVICE 2 OF 4. REFERENCE MFR. REPORTS # : 1627487-2013-220229, 1627487-2013-220231, 1627487-2013-220232. THE PT HAD TWO LEADS FROM THE SAME LOT. ON (B)(6) 2013, THE PT WAS REPROGRAMMED DUE TO INEFFECTIVE STIMULATION. X-RAYS REVEALED THAT THE LEADS FOR OFF LABEL USE HAD MIGRATED INTO A DIFFERENT LOCATION. ON (B)(6) 2013, THE PT UNDERWENT SURGICAL INTERVENTION TO REPOSITION THE LEAD. THE REPOSITIONING WAS UNSUCCESSFUL DUE TO SCAR TISSUE. IN TURN, THE PHYSICIAN CUT THE LEAD INTO PIECES AND REMOVED WHAT WAS ACCESSIBLE, TO IMPLANT THE NEW LEAD. THE NEW LEAD WAS PROGRAMMED ON (B)(6) 2013, RESULTING IN EFFECTIVE STIMULATION. FOLLOW UP REVEALED SURGICAL INTERVENTION RESOLVED THE PT'S ISSUES. ALL LEADS ARE BEING REPORTED BECAUSE IT IS UNKNOWN WHICH DEVICE HAD MIGRATED AND WAS EXPLANTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
470516 QUATTRODE SCS LEAD LGW ST. JUDE MEDICAL - NEUROMODULATION 3166 3530253

Patients

Seq Age Sex Outcome Treatment
1 62 YR Other IMPLANT:| SCS IPGS, MODEL: 3716 (X2)| SCS EXTENSION, MODEL: 3386| IMPLANT:| SCS EXTENSIONS, MODEL: 3346 (X2)| IMPLANT: