CPAP RECALL

Our law firm is currently reviewing claims brought by CPAP users who now

suffer from a wide variety of health complications.

Philips recalled millions of its CPAP, BiPAP and ventilator machines because of potential carcinogen and toxic chemical exposure. People have suffered serious complications including cancer, stroke, respiratory failure, lung damage, breathing difficulty, heart attack, and heart failure.

According to the FDA, the Philips Respironics CPAP and ventilator models that have been recalled include the following:

  • E30

  • DreamStation ASV

  • DreamStation AT, 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 V30 Auto


Register Your Recalled CPAP Here!