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 to chest pressure, cough, headaches and dizziness, lack of concentration, rashes in the abdomen, hands, arms and face, nausea and alterations in liver and kidneys.There was no report of serious patient harm or injury.There was no medical intervention required by the patient.
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