6/14/2021
Please read below regarding an important announcement related to certain CPAPs, BiLevel PAPs, and ventilators (including non-invasive and invasive ventilation) manufactured by Philips Respironics:
On June 14, 2021, Philips Respironics announced a voluntary recall for Continuous and Non-Continuous Ventilators (certain CPAP, BiLevel PAP and Ventilator Devices) due to two issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in these devices.
For information on the Recall Notice, a complete list of impacted products, and potential health risks, please visit: https://www.usa.philips.com/healthcare/e/sleep/communications/src-update.
Medical Services of America remains in communication with Philips concerning this product recall and we will do our best to relay any updated information to you as it is becomes available to us. Please reach out to your physician with any additional questions you may have regarding how this effects your therapy.
While we realize this is unwelcome news, rest assured our primary focus will always be our patient’s safety and health. If you have any additional questions, please click here.