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 vertigo from using the device.There is no allegation of serious or permanent harm or injury.The patient had stopped using the device because of the vertigo and under the recommendation of her doctor, she started reusing the device again and has started to experience the symptoms of vertigo again.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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