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 nose irritation, respiratory tract irritation, dizziness, headache, other, chronic cough and congestion, chest and lung pain (respiratory distress).Medical intervention was not specified.The manufacturer was made aware of this complaint through a representative of the customer.No patient information was provided.No additional information can be requested at this time.
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