Patient identifier field not sufficient to hold all digits, should read: (b)(4).A medtronic representative went to site to test the equipment.Representative was unable to replicate the reported issue.A system checkout was performed and the hardware, software, and instruments passed the system checkout.The system was found to be fully functional.No parts were replaced.No parts have been received by the manufacturer for evaluation.
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A medtronic representative reported that during catheter based procedure, non-invasive dynamic reference frame (drf) tracker was flickering in and out of red status in emitter details.Trackers was in green status more than red status, surgeon proceeded with the case.During troubleshooting, representative adjusted emitter placement, removed any external metal in the field and plugged the tracker into a different port.It was reported that all other instruments were tracking normally.The procedure was completed with the use of navigation.There was no delay to procedure.No impact on patient outcome.
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