Philips has investigated this complaint.According to the additional information collected the system was not in clinical use.The philips field service engineer (fse) inspected the system onsite and found that the system had loss power.Upon functional testing fse confirmed there was no failure identified in the device.The device has tested all specifications, the system was returned to use in good working condition.The codes were updated based on the investigation outcome.Health impact code was corrected.
|