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.The manufacturer received information alleged that the lid won't go into place and is not working properly.The user also alleged that the is giving half pressure which is not enough, noisy, air is coming out from all over the place and has a medical history of severe sleep apnea.There is no allegation of serious or permanent harm or injury.No medical intervention was required by the patient.The device was received by the manufacturer for evaluation.The service technician could not confirm the user's complaints of the lid won't go into place, device is not working properly, device giving only half pressure, noisy and air is coming out all over the place.There was no problem found.The device was scrapped due to age.
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