In a classic “two steps forward, one step back” situation, just as Philips is aiming to wrap up the repair-and-replace program for the 5.5 million respiratory devices it began recalling two years ago, ...

Philips sent updated instructions related to a problem with bilevel positive airway pressure, or BiPAP, machines that can cause interruption or loss of therapy. Philips recalled three models of BiPAP ...

Sleep apnea is a medical condition that affects an estimated 22 million Americans. Typical symptoms of sleep apnea include heavy snoring, excessive daytime sleepiness or fatigue, and difficulty with ...

Amsterdam, the Netherlands – On June 14, 2021, Royal Philips’ (NYSE: PHG, AEX: PHIA) subsidiary, Philips Respironics, initiated a voluntary recall notification* for certain sleep and respiratory care ...

Almost two full years into its Class I recall of more than 5 million respiratory devices, Philips has wrapped up safety tests covering nearly all of the affected models—and is reiterating its previous ...

Amsterdam, the Netherlands – royal philips (NYSE: PHG; AEX: PHIA), today provides an update on the comprehensive test and research program of its subsidiary Philips Respironics to assess potential ...

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 ...

Philips Respironics is recalling some of its BiPAP machines due to a plastic that can contaminate the machine and cause it to fail, according to the U.S. Food and Drug Administration (FDA). The ...

AMSTERDAM (dpa-AFX) - Philips, in an update on earlier announced voluntary CPAP, BiPAP and Mechanical Ventilator recall notification, said Sunday that the US Food and Drug Administration recently ...