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Current CPAP Product Recalls

In June 2021, after discovering a potential health risk related to the foam in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips Respironics issued a voluntary Field Safety Notice (outside U.S.) / voluntary recall notification (U.S. only).

Please visit Philips website for more information and to register your CPAP machine online to register your machine. By registering online, Philips will be able to confirm if your machine is part of the recall and arrange for any repairs/replacement units.  They will request the serial number of your CPAP machine which is located at the back/bottom of your machine.

Alternatively, should you not have access to email, please contact Philips directly at 1-877-907-7508

Public advisory: Philips Respironics alerts customers worldwide of updated instructions and labeling of specific sleep therapy masks that contain magnetic headgear clips due to potential risk of serious injury

Recall Notice – Labelling Amendment

SoClean has issued a recall notice regarding the label and instructions for use applicable to the SoClean 2 device.

To view the full notice, including a link to the updated user manual and instructions for use for the SoClean 2, please visit the SoClean website.