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 ...

Amsterdam, the Netherlands – Royal Philips’ (NYSE: PHG, AEX: PHIA) subsidiary, Philips Respironics, today provided an update on the remediation status in the US of the ongoing recall of certain sleep ...

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 ...

In June of 2021, Philips Respironics issued a recall for some of its CPAP and BiPAP machines. Now the U.S. Food and Drug Administration says the notification to users about the recall “have been ...

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 ...

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 ...

(News release) - 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 ...

SPRINGFIELD, Mo. – Philips Respironics recalled specific Continuous Positive Airway Pressure (CPAP), Bilevel Positive Airway Pressure (BiPAP), and Ventilators with a manufacturing date between 2009 ...

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 ...