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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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:
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The Department of Health, Disability and Ageing acknowledges First Nations peoples as the Traditional Owners of Country throughout Australia, and their continuing connection to land, sea and community. We pay our respects to them and their cultures, and to all Elders both past and present.
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