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 philips.com/src-update.
Additional helpful links from Philips: InfoHub Patient Portal Patient Journey Map
For information from the FDA regarding the Philips recall please click here.
For additional Clinical Information updated 7-8-2021 please click here.
Information for patients and caregivers who have received a DreamStation 2 as a replacement for your existing CPAP device click here.
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