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.
SleepSafe Drivers are in communication with the device manufacturer, 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 SleepSafe Driver’s primary focus is on your safety and health.
