The device trained customer received the device and reported the event was not duplicated in the biomed department.The biomed stated the nurse involved with the incident disposed of the consumable patient circuit including the exhalation filter, which the biomed felt was likely full water and the cause of this issue.The biomed also cycled the device for a week without incident and performed a preventative maintenance procedure, which the device passed all manufacture specifications.The customer has not requested a return good authorization (rga) for a vyaire evaluation of the device.At this time, vyaire medical has not received the suspect device for evaluation.In the event that the device is received for evaluation or additional information is received, a follow-up report will be submitted.
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