BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CHARGING SYSTEM

    MDR report key: 3182188 · Received June 14, 2013

    Report

    Report Number
    1627487-2013-04769
    Event Type
    Injury
    Date Received
    June 14, 2013
    Date of Event
    December 22, 2012
    Report Date
    May 22, 2013
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    LGW
    PMA / PMN Number
    P010032
    Removal / Correction Number
    1627487-07262012-001-C
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THIS CHARGER MODEL WAS ASSOCIATED WITH A FIELD CORRECTION. CORRECTIVE AND PREVENTIVE ACTION (CAPA). INVESTIGATION WAS PERFORMED. POCKET HEATING WAS 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. REF MFR REPORT: 1627487-2013-04767 AND 1627487-2013-04768. IT WAS REPORTED THE PT HAD RECEIVED A BURN WHILE RECHARGING THE IPG WITH THE CHARGING SYSTEM. THE PT REPORTED THE INCIDENT HAD HAPPENED 5 MONTHS BEFORE AND A SCAB FORMED AND MORE RECENTLY THERE WAS A SCAR. THE PT REPORTED THE IPG WAS SHALLOW UNDER THE SKIN. IT WAS ALSO REPORTED THE SYSTEM WOULD TURN ON RANDOMLY AND A SHOCKING SENSATION WOULD OCCUR IN HER LEFT LEG WHICH WOULD CAUSE HER TO DRAW HER LEGS TOWARD HER CHEST. THE PT WAS NO LONGER RECEIVING EFFECTIVE STIMULATION AND HAD DISCONTINUED THE USE OF THE SCS SYSTEM. IT WAS REPORTED THE PHYSICIAN PLANNED TO EXPLANT THE SYSTEM. ON 08/01/2012, ST JUDE MEDICAL, NEUROMODULATION DIVISION, SENT FIELD ACTION LETTERS TO PTS RELATED TO HEATING WHILE CHARGING AND RAISED AWARENESS OF THIS ISSUE TO PTS. 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
    270758 CHARGING SYSTEM SCS CHARGING SYSTEM LGW ST. JUDE MEDICAL - NEUROMODULATION 3721 3213352

    Patients

    Seq Age Sex Outcome Treatment
    1 50 YR Other