The manufacturer received a voluntary medwatch (mw5116052) 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 shortness of breath, brain fog, headaches, awakening from the nigh terror, pain memory loss, the patient required no medical intervention.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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