Voluntary Recall Information

Ventilation device remediation progress updates

 

We are committed to remediating affected ventilators in alignment with the relevant competent authorities, and continue to work with independent testing laboratories to conduct extensive testing and analysis of the affected devices.

 

Philips Respironics will communicate with DMEs directly throughout the remediation process. If you are a patient or caregiver with an affected Philips Respironics ventilation device, you do not need to take any action. All ventilation remediation will be done via your DME.

Sleep therapy device remediation progress updates

 

Globally, we have remediated 99% of actionable* sleep therapy device registrations to date. 

Continuing to remediate new and existing registrations remains our priority. We will make multiple attempts to ensure we have the information needed to place an order, and will provide responding patients with remediation options. 

*Actionable registrations are those that contain the necessary information needed to complete the remediation and are not awaiting further information.

** Remediated patients include those who have received a new, recertified or an alternative device sent as replacements for affected units, those who have had devices shipped to their DME directly handling patient remediations, or those who received financial payment.