During review of the patient¿s programming history available in the manufacturer¿s database, it was identified that a programming anomaly occurred.A system diagnostic test was performed, which changed the patient's settings.Manufacturer labeling indicates to perform a final interrogation to confirm intended settings prior to patients leaving the clinic.The settings were interrogated again and programmed to 0/20/500/30/60/1/500/30 on (b)(6) 2015 but not all settings were corrected.The normal output current was left disabled and the magnet output current was left at 1.0 ma.
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