Philips CPAP/BiPAP Recall Information
In June 2021, Phillips issued a nationwide, voluntary recall of parts of CPAP and BiPAP devices listed here:
- Philips Respironics CPAP and BiPAP Machine Models are: Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent, BiPAP V30, and BiPAP A30/A40 Series device models
Should I still use my machine?
HPP encourages all members who use a CPAP or BiPAP machine to talk to your doctor who ordered your machine as soon as possible. Your doctor will determine the most appropriate options for your continued treatment.
How can I tell if my CPAP/BiPAP device is affected?
The manufacturer is asking everyone who uses a Phillips CPAP or BiPAP to register their machine to determine if their device is affected. Once you register the machine, you get more information about if your device will need to be replaced.
Go to www.Philips.com/SRC-Update or call 877-907-7508 to begin the registration process.
How long will it take to get a new part for my machine?
This is a nationwide, voluntary recall, so the timeline for replacement is unclear at this time.
HPP is monitoring this recall very closely and will inform members and providers of any updates. If you have any questions, please contact HPP by calling the Member Relations number on the back of your member ID card.