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 sinus inflammation, respiratory discomfort, heavy secretions (nose/throat), asthma symptoms, eye irritations, and headaches.The patient had a samu visit (service d¿aide médicale urgente (urgent medical aid service) on (b)(6) 2020.Ent (ear, nose, and throat) and respiratory problems not identified.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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