The manufacturer was contacted in reference to the voluntary field safety notice / recall notification related to the sound abatement foam in certain cpap, bipap, and mechanical ventilator devices.There is no allegation of serious or permanent harm or injury.No medical intervention was required by the patient.A device was returned to the manufacturer for evaluation to the voluntary field safety notice / recall notification related to the sound abatement foam in certain cpap, bipap, and mechanical ventilator devices.During the evaluation of the device, the third-party service center visually inspected the device and has no visualization of foam particles.In addition to above findings, the complaint of smoke odor was confirmed.The device has also error codes, which is the error code numbers was 83x5.The device was routed to scrap.At this time, no further investigation can be performed.If any additional information is received, a follow up report will be filed.
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