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Air Liquide would like to inform our patients of the statement released by the Therapeutic Goods Administration (TGA) on July 6, 2021 following their review with Philips regarding the sound abatement foam in their CPAP, BiLevel and ventilator devices. The full statement can be found here: https://www.tga.gov.au/alert/philips-recall-action-cpap-bi-level-pap-devices-and-mechanical-ventilators?fbclid=IwAR0zyMiaXH7-lQSs_gyzoviQ-RMAvdqhWFjkXcAlKZORp_3jQ6TaGIYFGWw As advised by the TGA, patients need to register their device on the Philips support website: https://www.philips.com.au/healthcare/e/sleep/communications/src-update This will allow Philips to contact you to organise the corrective actions or a replacement device. If you have any questions or concerns, contact Philips Electronics Australia Ltd on 1800 009 579.