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 skin irritation, respiratory tract irritation, dizziness and or headache, hypersensitivity,nausea,vomiting, asthma (new worsening), inflammatory response, lung disease.Medical intervention was not specified.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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