Get all the latest news on coronavirus and more delivered daily to your inbox. Sign up here. As doctors face a shortage of ventilators that are crucial for treating coronavirus patients with ...

The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines. A Class I recall means the FDA has ...

As hospitals in New York City and beyond are facing a shortage of mechanical ventilators for COVID-19 patients in critical care, many are turning to readily available CPAP and BiPAP machines as a ...

Certain Philips Respironics DreamStation breathing devices, commonly used for treating sleep apnea, may deliver the incorrect prescription or no therapy at all, the FDA warned in a recall announcement ...