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 patient alleges eye irritation, dizziness, skin irritation, respiratory tract irritation, dizziness, headache, hypersensitivity, nausea, vomiting, inflammatory response, lung disease, and asthma (new or worsening).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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