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 nose irritation, lung damage, kidney cyst, afib (atrial fibrillation), pneumonia, and copd (chronic obstructive pulmonary disorder).The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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