Philips CPAP
& Ventilator Machines

Register your interest to
join the Philips CPAP, BiPAP
& mechanical Ventilator
Machines Class Action

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Philips CPAP, BiPAP & Mechanical Ventilator Machines Class Action

legal proceedings have been issued

Various models of CPAP, BiPAP and mechanical ventilator machines made by Philips have been recalled due to safety concerns. 

Carbone Lawyers wants to hear from members of the public who may have been put at risk and are interested in joining a class action claim against Philips. 

Australia’s Therapeutic Goods Administration (TGA) has listed 18 devices for recall after it was discovered that the polyurethane foam within the machine had the potential to degrade and cause the consumer to inhale and ingest its particles, which is feared may cause cancer and other health issues.

If you have been using one of the devices listed, please complete this enquiry. You will receive a questionnaire to register your interest.

All devices manufactured before 26 April 2021 All serial numbers
Continuous Ventilator, Minimum Ventilatory Support, Facility Use
E30 (Emergency Use Authorization)
Continuous Ventilator, Non-life supporting
DreamStation ASV

DreamStation ST, AVAPS

SystemOne ASV4

C-Series ASV

C-Series S/T and AVAPS

OmniLab Advanced+
Noncontinuous Ventilator
SystemOne (Q-Series)


DreamStation Go

Dorma 400

Dorma 500

REMstar SE Auto

Continuous Ventilator
Trilogy 100

Trilogy 200
Continuous Ventilator, Minimum Ventilatory Support, Facility Use
A-Series BiPAP V30 Auto
Continuous Ventilator, Non-life supporting
A-Series BiPAP A40

A-Series BiPAP A30