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Philips recall action for CPAP, Bi-Level PAP devices and mechanical ventilators collection
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:
- contact Philips Electronics Australia Ltd support hotline on 1800 009 579
- visit www.philips.com/src-update.
- Philips’ recall action for sleep apnoea and respiratory care machines – Final chance to register for a replacement deviceMedia releasesIf 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 this recall action. Register your machine for repair or replacement to avoid any potential risks.
- Safety alertsSafety alert relating to CPAP and BiPAP face and nasal masks that contain magnets which may cause active implantable devices to malfunction
- Philips’ recall action for sleep apnoea and respiratory care machines – have you registered for a replacement?Media releasesThe TGA is calling for anyone using a Philips Continuous Positive Airway Pressure (CPAP) machine or a Bi-level Positive Airway Pressure (Bi-Level PAP) machine to see if they are affected by the recall action.