On June 14, 2021, Philips Respironics initiated a voluntary recall notification for specific models of continuous positive airway pressure (CPAP), bilevel positive airway pressure (BPAP), and mechanical ventilator devices to ensure patient safety.

The recall is to address potential health risks related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in certain devices. Please see the recall notification in the Philips Respironics website for additional information and a complete list of models.

https://www.usa.philips.com/healthcare/e/sleep/communications/src-update

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