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), lung disease, reduced cardiopulmonary reserve, copd, hospitalization for double lung pneumonia.In addition, the following non-serious injury of eye irritation, nose irritation, skin irritation, respiratory tract irritation, dizziness and/or headache, nausea / vomiting, inflammatory response, severe coughing and choking and chronic respiratory infections.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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