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 an issue related to a cpap device's sound abatement foam.The patient has alleged chronic cough.The patient also alleges visualization of smoke from the device.There was no report of serious patient harm or injury.There was no medical intervention was required by the patient.The device was returned to the manufacturer but not yet evaluated.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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