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 difficulty breathing and seizures.The patient states needing unit as they stop breathing in sleep, has been having health issues, and is hard for them to breathe if they discontinue the unit.No medical intervention was mentioned for the reported events.The manufacturer's investigation is ongoing.A follow-up report will be submitted when the manufacturer's investigation is complete.
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