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 voluntary medwatch (mw5148205).The manufacturer received information alleging an issue related to a dreamstation cpap device's sound abatement foam.The patient has alleged of asthma, rashes, shortness of breath, migraines, blurry vision, chest pain and heart palpitations.No medical intervention was required by the patient.The device has not yet been returned to the manufacturer for evaluation.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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