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 an issue related to a cpap device's sound abatement foam.The patient has alleged colon cancer.The patient also alleged of having headaches and severe sinus inflammation.The manufacturer's investigation is ongoing.A follow up report will be submitted when the manufacturer's investigation is complete.
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