He 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 of having eye irritation, nose irritation, skin irritation, dizziness, headache, nausea, vomiting, kidney disease/toxicity, and lung disease.There was no report of serious or permanent patient harm or injury.The manufacturer's investigation is ongoing.A follow up report will be submitted when the manufacturer's investigation is complete.
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