Philips recall action for CPAP, Bi-Level PAP devices and mechanical ventilators collection

Safety hazard caused by foam degradation and emissions

This recall action was first published on our website on 18 June 2021 and updates from June 2021 to July 2022 are contained within the first recall. Further updates are published to this collection.

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About this recall action

The TGA is working with Philips on its global recall action for Continuous Positive Airway Pressure (CPAP), Bi-Level Positive Airway Pressure (Bi-Level PAP) devices and mechanical ventilators. Risks are posed by the polyester-based polyurethane (PE-PUR) sound abatement foam component in these devices. The majority of the affected devices are in the first-generation DreamStation product family.

We continue to work with Phillips to ensure that information is made available through on the TGA website and from Phillips directly to customers. For questions about this issue:

contact Philips Electronics Australia Ltd support hotline on 1800 009 579
visit www.philips.com/src-update - external site.

9 result(s) found, displaying 1 to 9

Update on product defect A40/30 BiPAP Series

4 June 2024

Market actions

The affected bi-level positive airway pressure (BiPAP) devices may stop providing therapy on an intermittent or permanent basis and the ‘Ventilator Inoperative’ alarm will sound.
Philips’ recall action for sleep apnoea and respiratory care machines – Final chance to register for a replacement device

7 December 2023

Media releases

If you use a Philips Continuous Positive Airway Pressure (CPAP) machine or a Bi-level Positive Airway Pressure (Bi-Level PAP) machine you may be affected by this recall action. Register your machine for repair or replacement to avoid any potential risks.
Updated information for repaired Philips Respironics Trilogy 100 devices

21 December 2022

Safety alerts

Philips Respironics (the manufacturer) detected two problems with corrected Trilogy 100 ventilators
CPAP and BiPAP face and nasal masks that contain magnets

24 November 2022

Safety alerts

Safety alert relating to CPAP and BiPAP face and nasal masks that contain magnets which may cause active implantable devices to malfunction
Philips recall action for CPAP, Bi-Level PAP devices and mechanical ventilators - Update on Trilogy 100 Ventilators

11 November 2022

Market actions

Update on Trilogy 100 Ventilators
Philips’ recall action for sleep apnoea and respiratory care machines – have you registered for a replacement?

7 November 2022

Media releases

The TGA is calling for anyone using a Philips Continuous Positive Airway Pressure (CPAP) machine or a Bi-level Positive Airway Pressure (Bi-Level PAP) machine to see if they are affected by the recall action.
Philips' face and nasal masks with magnetic clips

7 November 2022

Market actions

Philips Respironics patient interface devices (face and nasal masks) with magnetic clips - New warnings
Philips recall action for CPAP, Bi-Level PAP devices and mechanical ventilators - Update on BiPAP settings

26 September 2022

Market actions

Update on BiPAP settings issues and recall progress
Philips recall action for CPAP, Bi-Level PAP devices and mechanical ventilators

18 June 2021

Market actions

This page contains the original recall in June 2021 and progress updates to 2024.

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Philips recall action for CPAP, Bi-Level PAP devices and mechanical ventilators collection

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About this recall action

Update on product defect A40/30 BiPAP Series

Philips’ recall action for sleep apnoea and respiratory care machines – Final chance to register for a replacement device

Updated information for repaired Philips Respironics Trilogy 100 devices

CPAP and BiPAP face and nasal masks that contain magnets

Philips recall action for CPAP, Bi-Level PAP devices and mechanical ventilators - Update on Trilogy 100 Ventilators

Philips’ recall action for sleep apnoea and respiratory care machines – have you registered for a replacement?

Philips' face and nasal masks with magnetic clips

Philips recall action for CPAP, Bi-Level PAP devices and mechanical ventilators - Update on BiPAP settings