PHILIPS RESPIRONICS RECALL INFORMATION

• We want to make you aware of an important development related to certain CPAPs, BiLevel PAPs, and ventilators (including non-invasive and invasive ventilation) manufactured by Philips Respironics.  Please be sure to read this information in detail.
• 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, visit www.philips.com/src-update.
• Apnix is in communication with Philips about this recall and we will do our best to communicate information to you, our patients.
• At this point, Philips has not provided the timing of the availability of potential future product replacement. 
• 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
• We realize this is unwelcome news, but please be assured that Apnix’s primary focus is on your safety and health.