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On 6 July 2021, the Therapeutics Goods Administration formally issued a recall for the Phillips CPAP, BiPAP and mechanical ventilator devices ‘in response to risks posed by the polyester-based polyurethane (PE-PUR) sound abatement foam component in these goods’.

Slater and Gordon understand there are a significant amount of people in Australia who use these devices, who are impacted by this recall.

If you are a person affected by the recall of Philips CPAP, BiPAP or mechanical ventilator devices, Slater and Gordon Lawyers would be interested in hearing from you. Please fill in your details below and Slater and Gordon Lawyers will be in contact with you in due course.

Last updated 31st August 2021.