Connected BiPAP A40 EFL ventilator is the first to help healthcare professionals screen, detect, and abolish expiratory flow limitation to reduce work of breathing in COPD patients with abnormally ...

FDA posted details this week regarding the most recent recall on ventilators made by Philips, prompting widespread media coverage Tuesday. This recall, however, is the same one the agency previously ...

Amid a yearlong effort to recall more than 5 million of its respiratory devices distributed around the globe, Philips has also faced two separate recalls pertaining to its high-flow oxygen therapy V60 ...

Philips Respironics, Inc. has issued updated instructions for the use of its OmniLab Advanced+ (OLA+) Ventilator because of its demonstrated failure in the ventilator inoperative alarm that can cause ...

Philips identified an issue within the internal power mechanism of its V60, V60 Plus and V680 ventilators where an energy fluctuation could force a reboot of the backup alarm controller, which might ...

AMSTERDAM, June 14 (Reuters) - Dutch medical equipment company Philips (PHG.AS), opens new tab has recalled some breathing devices and ventilators because of a foam part that might degrade and become ...

Philips is recalling breathing devices and ventilators due to foam that might degrade and become toxic, possibly causing cancer, the Dutch medical equipment maker said on Monday. The recall involves ...

Philips engages manufacturing partners Flex Ltd. (NASDAQ: FLEX) and Jabil (NYSE: JBL), as well as other partners, to further expand its hospital ventilator assembly lines and strengthen its supply ...

AMSTERDAM, Aug 31 (Reuters) - Philips (PHG.AS), opens new tab said the U.S. Department of Health had cancelled most of an order for 43,000 ventilators, leading the Dutch medical equipment maker to cut ...