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 previously received a voluntary medwatch report (mw5146874) from a user alleging the dreamstation auto cpap caused headaches, nausea, vasovagal responses, vomiting, skin condition, tightness of chest and throat.Gas reflex and inflammation, chronic fatigue etc.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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