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 alleges chest tightness, dizziness, and cough.The patient did not mention did not mention the visualization of particles; however, they are worried about the effects the device has on their body especially since they were not notified of the recall.There is no allegation of serious or permanent harm or injury.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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