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 alleging device is not performing properly which is causing several issues for the patient.The patient reports not being rested, always tired, experiencing constant cough, dry and sore nose.The patient states device is not using water and she does not know why.She puts water in, and nothing is gone in the morning, the levels stay the same.There is no allegation of serious or permanent harm or injury.No medical intervention was required by the patient.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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