07/15/2021
Recall: Philips CPAP, BiPAP machines
Philips Respironics announced a voluntary recall for certain CPAP, BiLevel PAP machines due to issues related to deterioration of the sound abatement foam used in these devices. This recall affects CPAP and BiLevel PAP devices manufactured prior to April 26, 2021.
If you are a Veteran that uses a Philips Respironics CPAP or BiPAP device, continue to use your device as prescribed. You should register your device at https://www.philipssrcupdate.expertinquiry.com.
Philips Respironics will send you a new device when one is available.
Philips is deploying a permanent corrective action to address the two (2) issues described in the Field Safety Notification.* Please see the list of affected devices and initiate the registration process below.