Which CPAP Machines Are on Recall?

As of June 30, 2021, the following Philips Respironics CPAP machines are on the FDA recall list:

• E30 (Emergency Use Authorization)
• DreamStation ASV
• DreamStation ST, AVAPS
• SystemOne ASV4
• C-Series ASV
• C-Series S/T and AVAPS
• OmniLab Advanced+
• SystemOne (Q-Series)
• DreamStation
• DreamStation Go
• Dorma 400
• Dorma 500
• REMstar SE Auto
• Trilogy 100
• Trilogy 200
• Garbin Plus, Aeris, LifeVent
• A-Series BiPAP Hybrid A30 (not marketed in US)
• A-Series BiPAP V30 Auto
• A-Series BiPAP A40
• A-Series BiPAP A30

For more information, please see the official FDA statement.