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 alleges eye irritation, nose irritation, respiratory tract irritation, dizziness and/or headache in coughing.Increase in hypertension, now sleeps sitting on couch in other, choking up food, increase reclining position instead of lying down.Increase in thirst for water, preferably alkaline water.There was no report of medical intervention.No additional information can be requested at this time.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.The device has not yet been returned to the manufacturer for evaluation and there is no contact information to gain additional information on the device.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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