It was reported that, while in use on a patient, a 980 ventilator generated a severe occlusion error message.The patient was removed from the ventilator and placed on an alternate ventilator.The patient was not harmed or injured as a result of the reported event.The service engineer (se) inspected the device and found alarms in the memory logs relevant to the reported issue; however, was not able to duplicate the reported issue.The se performed calibrations and extended self-testing on the device and all tests passed.
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