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In November 2022, the TGA reminded Australian customers to register with Philips to have their devices replaced. Philips will be closing their registration process in early 2024.
We ask all customers who have not yet registered their devices to do so as soon as possible. This action only applies to devices purchased prior to 1 January 2023.
If you have not registered and 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 the current recall action. If so, you must register your machine for repair or replacement to avoid any of the potential risks.
Have you registered your machine yet, or do you care for someone who needs to register? Please check against the list of affected devices and register at Philips Respironics Sleep and Respiratory Care devices.
If left unfixed, the foam used in the blower box to reduce the noise of the machine may degrade into particles and release certain chemicals or gases which may be inhaled or ingested. Long term continued use of affected machines may lead to symptoms such as headaches, nausea, inflammatory responses, asthma and possible carcinogenic effects.
Both CPAP and BiPAP machines are commonly used to treat sleep apnoea and other health conditions that impair breathing, especially during sleep.
In July 2021 Philips began a global corrective action for certain CPAP and BiPAP sleep and respiratory care machines. The TGA has continued to closely monitor the progress of the recall and work with Philips to provide comprehensive information on the TGA website and from Philips directly to registered customers.
For full information, including the list of affected devices, please see the Philips Recall action page.
Contact for members of the media:
Email: news@health.gov.au
Phone: 02 6289 7400
