Affected Devices
Philips Respironics 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.
For more information on this Field Safety Notification*, please visit
Philips.com/SRC-Update
URGENT: Field Safety Notification*
If you are a physician, please click here for more information. If you are a Patient, Device User, Caregiver, DME, Distributor, Pharmacy, or Institution, begin your registration below:
This is a list of products affected globally. For a list of products affected in your country please click here
Items marked with an asterisk (*) are required.
* Highlighted field(s) is/are required.
I am a: *
Choose your Country: *
Based on your country selection, your DME/Distributor/Pharmacy/Institution is responsible for managing the recall on your behalf.
* In Australia this is an Urgent Product Defect Correction and in New Zealand this is a Recall for Product Correction
Registration for affected CPAP and BiPAP devices in the US and Canada closed on December 31, 2024. The Patient Portal will remain open for registered US patients until June 30, 2025. Learn more