It was reported to philips that the device experienced a pacer equipment malfunction.The customer requested that the device be returned for bench repair.Upon evaluation of the device, the reported issue was confirmed and the cause was traced to a faulty power pca.The defective part was ordered for replacement at bench repair.Based on the conclusion of the evaluation, it was determined that this was a malfunction of the power pca.The part was replaced and the device passed all performance assurance testing.The device was returned and remains at the customer site.There is no indication of a systemic problem.No further investigation or action is warranted.
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