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, nose irritation, kidney disease/toxicity, lung disease, sinusitis, bronchitis, pharyngitis, thyroid nodule.While using the device.There was no report of medical intervention being required.The manufacturer was made aware of this complaint through a representative of the customer.At this time, no further investigation can be performed.If any additional information is received, a follow up report will be filed.
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