The manufacturer received a voluntary medwatch (mw5147524) in reference to the field safety notice/recall notification related to the sound abatement foam in certain cpap, bipap, and mechanical ventilator devices.The manufacturer received information alleging severe cough, shortness of breath, asthma, lung infections, fluid on lungs, pneumonia and respiratory failure.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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