URGENT: Field Safety Notification*

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 included devices and initiate the registration process below.

For more information on this Field Safety Notification*, please visit Philips.com/SRC-Update

Included Devices

This is a list of products included globally. The field safety notification provided information on the possibility that a potential risk could arise and the resulting field safety corrective action, a preventing measure to prevent the risk of a serious incident, to counteract it. However, neither the field safety notification nor the field safety corrective action, nor the fact that a unit is included in the field safety notice, allows any conclusion as to whether a risk mentioned in the filed safety notification could actually materialize in the unit. Rather, the test results for the units have shown that a health risk is unlikely to be expected. For a full list of products included in the field safety notification in your country, please click here.

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:

* In Australia this is an Urgent Product Defect Correction and in New Zealand this is a Recall for Product Correction