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 ...

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 ...

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 ...

More than a year after the official start of the ongoing Class I recall that has sent revenues plummeting and affected millions of CPAP and BiPAP machine and ventilator users around the world, ...

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 ...

Though Philips recently expanded its ongoing respiratory device recall to include around 5.2 million machines, that list left off a handful of ventilators that weren’t affected by the original issue.

MARKHAM, ON, Canada--(BUSINESS WIRE)--Royal Philips (NYSE: PHG, AEX: PHIA) today announced the Canadian launch of the Philips Respironics V680 Ventilator for hospital respiratory care, offering both ...

Philips on Monday announced that it will recall several ventilators and CPAP breathing machines after it discovered that a small foam component in the machines might degrade and be inhaled, a move ...

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 ...