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 has alleged nose irritation, respiratory tract irritation, dizziness, headache, asthma, lung disease, body pains upon light touch, leg pain which restricts walking and ambulatory movement.Medical intervention was not specified.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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