FDA Adverse Event Injury Summary report: N

CHARGING SYSTEM

MDR report key: 2934440 · Received January 28, 2013

Report

Report Number
1627487-2013-05146
Event Type
Injury
Date Received
January 28, 2013
Date of Event
January 8, 2013
Report Date
January 9, 2013
Manufacturer
ST. JUDE MEDICAL - NEUROMODULATION
Product Code
LGW
PMA / PMN Number
P010032
Removal / Correction Number
1627487-07262012-001-C
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
WA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THIS CHARGER MODEL WAS ASSOCIATED WITH A FIELD CORRECTION. MANUFACTURER'S EVALUATION: CORRECTIVE AND PREVENTIVE ACTION (CAPA) INVESTIGATION WAS PERFORMED. RESULTS: POCKET HEATING WAS CONFIRMED. THE INVESTIGATION FOR (B)(4) ASSOCIATED WITH HEATING WHILE CHARGING (POCKET HEATING) CONCLUDED THAT THE CHARGER WAS CAPABLE OF TRANSFERRING ENERGY TO THE IPG AT A RATE THAT WOULD CAUSE HEATING OF THE IPG AND/OR CHARGING WAND OF SUFFICIENT ELEVATED TEMPERATURE TO CAUSE PAIN AND BURNS. THE HEATING WHILE CHARGING WAS DETERMINED TO BE EXACERBATED BY OFF-AXIS CHARGING OF SHALLOW IMPLANTED IPGS AND THAT ALL CHARGERS WERE CAPABLE OF ELEVATED HEATING. 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

REFERENCE MFR REPORTS # 1627487-2013-05144 AND 1627487-2013-05145. THE PATIENT HAS TWO LEADS (FROM THE SAME LOT). IT WAS REPORTED THE PATIENT IS EXPERIENCING HEATING AND DISCOMFORT AT THE IPG SITE WHILE RECHARGING. IT WAS ALSO REPORTED THE PATIENT IS NOT RECEIVING PAIN RELIEF FROM STIMULATION. REPROGRAMMING ATTEMPTS HAVE BEEN UNSUCCESSFUL. SURGICAL INTERVENTION IS PENDING TO ADDRESS THE ISSUES. ON (B)(4) 2012, ST. JUDE MEDICAL, NEUROMODULATION DIVISION, SENT FIELD ACTION LETTERS TO PATIENTS RELATED TO HEATING WHILE CHARGING AND RAISED AWARENESS OF THIS ISSUE TO PATIENTS. AN INCREASE IN PRIOR NON-REPORTED HEATING WHILE CHARGING EVENTS AND OTHER NON-REPORTED EVENTS WAS EXPECTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
37350 CHARGING SYSTEM SCS CAHRGING SYSTEM LGW ST. JUDE MEDICAL - NEUROMODULATION 3721 3478450

Patients

Seq Age Sex Outcome Treatment
1 62 YR Required Intervention SCS ANCHORS: MODEL 1192 (X2)| IMPLANT: