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Philips Respironics Recall Information

June 18, 2021

To Our Valued Patients and Customers,

Please be aware of an important development related to certain CPAPs, BiLevel PAPs, and ventilators (including non-invasive and invasive ventilation) manufactured by Philips Respironics.  We ask that you read this information in detail.  

Philips Respironics announced a voluntary recall for Continuous and Non-Continuous Ventilators (certain CPAP, BiLevel PAP and Ventilator Devices) on June 14, 2021.  The recall is 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, visit philips.com/src-update.

UHS Home Care is in communication with Philips about this recall and we will do our best to communicate information to you, our patients.

Please also reach out to your physician with any additional questions you may have regarding your therapy.

You can access the Philips Q&A at https://www.usa.philips.com/healthcare/e/sleep/communications/src-update#questions_and_answers.

Please be assured that UHS Home Care’s focus is on the safety and well-being of our patients and customers.  Visit philips.com/src-update for future updates.