Philips Respironics CPAP, BiPAP and Ventilator Device Recall Update

Gray top section: <b>September 2021 –</b> Philips received U.S. Food and Drug Administration (FDA) authorization for rework of affected first-generation DreamStation devices, which consists of replacement of the PE-PUR sound abatement foam with new material.

Philips started shipping replacement devices to those who registered their recall devices. Please contact your dispensing durable medical equipment provider for support once the replacement device is received.

For the most current Philips recall information and to register your device please visit:

https://www.usa.philips.com/healthcare/e/sleep/communications/src-update

or call 877-907-7508

If you choose to discontinue use of your recalled machine, we suggest:

do not sleep on your back and place a pillow behind your back to prevent you from rolling over.
avoid alcohol, sedatives, or narcotics near bedtime.
discuss alternatives like adjustable oral appliances, oxygen or surgery at your next appointment.

We will continue to update this message as soon as new information becomes available.