The Device's Failure to Switch Power Sources Poses Risks of Ventilation Disruption, the FDA Warns. The US Food and Drug Administration (FDA) has taken decisive action by issuing a Class I recall for Draeger Medical’s Oxylog 3000 Plus Emergency and Transport Ventilator, citing potential serious harm or even death. Draeger … [Read more...] about FDA Recalls Draeger’s Oxylog 3000 Ventilator Due to Power Rerouting Concerns