FDA Adverse Event Injury Summary report: N

CHARGING SYSTEM

MDR report key: 3961312 · Received July 18, 2014

Report

Report Number
1627487-2014-03482
Event Type
Injury
Date Received
July 18, 2014
Date of Event
June 23, 2014
Report Date
June 23, 2014
Manufacturer
ST. JUDE MEDICAL, NEUROMODULATION
Product Code
GZB
PMA / PMN Number
P010032
Removal / Correction Number
1627487-07262012-001-C
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, 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. RESULT: - POCKET HEATING CONFIRMED. THE INVESTIGATION FOR CAPA (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

DEVICE 3 OF 3 - REFERENCE MFR. REPORTS: 1627487-2014-03480 AND 1627487-2014-03481: IT WAS REPORTED THE PATIENT EXPERIENCES HEATING WHILE CHARGING, INCREASED RECHARGE BURDEN AND LEG PAIN. AN SJM REPRESENTATIVE WAS UNABLE TO RESOLVE THE ISSUES WITH REPROGRAMMING AND REPLACING THE CHARGING SYSTEM. ON 08/01/2012 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. DUE TO THE NATURE OF LITIGATION THESE ALLEGATIONS CANNOT BE CONFIRMED OR REJECTED. 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.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
421075 CHARGING SYSTEM SCS CHARGING SYSTEM GZB ST. JUDE MEDICAL, NEUROMODULATION 3721 2896354

Patients

Seq Age Sex Outcome Treatment
1 54 YR Other