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Phillips Respironics
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.
We are currently reviewing our record to identify distributed equipment impacted by the voluntary recall.
Please call contact our office with any questions 706-275-6600
Recall Information
Philips is committed to rectifying this issue through a robust and comprehensive repair and replacement program. We have established a claims processing and support center to assist you.
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