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 from the legal department with the patient alleging allegations of nose irritation, respiratory tract irritation, dizziness or headache, asthma (new or worsening), lung disease, and eye irritation.The patient had a visit with a swallowing specialist.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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