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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.

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:

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