Philips Respironics has updated use instructions for three bi-level positive airway pressure machines, according to a recall statement posted by the US FDA. The recall does not include removal of the ...

FDA has issued a Class I recall for a handful of Philips Respironics BiPAP ventilator devices following 13 reported injuries and eight deaths connected to the models. Impacted ventilator models ...

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 ...

March 7 (Reuters) - Respironics Inc. said U.S. regulators granted approval to market its ventilatory support device, BiPAP autoSV, for sleep-disordered breathing patients. The company said the device ...

A custom-made valve fits to the top of full-face masks, where the snorkel is meant to go, allowing them to connect to standard BiPAP machines that feed pressurised air into masks AFP / Kenzo ...

Co announces that the FDA granted 510(k) clearance of the BiPAP autoSV device, which is intended to provide noninvasive ventilatory support to treat adult patients with Obstructive Sleep Apnea and ...

The U.S. Food and Drug Administration on Friday announced the recall of certain Philips Respironics devices designed to help people with breathing conditions keep breathing at a regular rhythm. The ...