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 asthma (new or worsening) and liver disease/toxicity, eye, nose and respiratory tract irritation, severe eye pain, very dry nostrils, severe pain in both lungs, breathing difficulties.No other clinical information or medical interventions were reported.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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