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.

DME/Distributor/Pharmacy/Institution

Patient/Device User/Caregiver

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