Medical Device Recall Information

Philips Respironics Sleep and Respiratory Care devices

Registration for affected CPAP and BiPAP devices in the US and Canada closed on December 31, 2024.

I would like to speak with someone.

We are experiencing a high volume of calls and wait times may be longer than normal.

Recall of CPAP, BiPAP and Ventilators relating to the PE-PUR sound abatement foam

I need to update my registration information.
Updating contact information (including address), or to cancel a registration.

877- 907-7508
(M-F 8a-5p EST)

I have a question about the status of my replacement device related to the June 2021 recall of certain Philips Respironics ventilators in Canada.

In most cases, your Durable Medical Equipment provider (DME) will handle all aspects of your replacement device remediation. If you do not have a DME, or if you have other questions, please contact us via email using the link to the right.

Email us

I have general DreamMapper questions or DreamMapper connection issues.

855-699-6276
(M-F 8:30a-5p EST)

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