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 particles in the patient's airway came from the device.The device had a strange odor and caused the patient to lose oxygen to the brain, seizure, and lose consciousness.There was no medical intervention specified.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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