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 patient alleges waking up with severe dry mouth.The patient sought medical attention and was treated for inflamed throat and tonsil infection.The humidifier stopped working and a week later the cpap quit working.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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