June 30, 2021. The U.S. Food and Drug Administration (FDA) is alerting people who use Philips Respironics ventilators, BiPAP, and CPAP machines and their health care providers that Philips Respironics has recalled certain devices (see table below) due to potential health risks. 

Click here to go to the FDA website for more information

Click here for the UK information from Philips