Important Recall of Philips PAP Units

Jun. 14, 2021: Philips, the medical equipment manufacturer announced a voluntary recall of most of their PAP units in the market. The problem is linked to use of a sound abatement foam made of Polyurethane Polyester (PE-PUR). Philips is recalling the equipment because this sound abatement foam can cause potential health risks. The complaint rate is low (0.03% in 2020).

Clinique Sommeil Sante is not responsible for this recall but rest assured that we are monitoring the situation very closely and will continue to communicate the latest news on our website.

Philips recommends that all PAP users stop their treatment and consult their treating physician or Respirologist to discuss alternative to the PAP treatment. Please see American Thoracic Society’s recommendations:

https://www.thoracic.org/patients/patient-resources/recommendations-for-sleep-and-critical-care-medicine-professionals-regarding-philips-recall-notice.php

Philips will replace or repair all equipment, but we don’t have an expected date. It is recommended to register your equipment by clicking on the following link:

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

If you encounter any problems or are unable to register your machine, please communicate with us and one of our team members will register it for you.