Once again, Philips has been hit with an FDA Class I label for a correction to certain of its respiratory support devices. The V60 and V60 Plus devices escaped that longstanding recall since they ...

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There seems to be no limit to Philips’ ventilator safety woes. Nearly a full year after initiating a recall of many of its respiratory devices that has since stretched to encompass around 5.2 million ...

Philips Respironics recalled all V60 and V60 Plus Ventilators on June 3 over a power issue that may cause the devices to shut down without an alarm. The FDA classified the recall as a class 1, the ...

AMSTERDAM (dpa-AFX) - Philips Respironics, a unit of Dutch consumer electronics giant Philips Electronics NV, has recalled V60/V60 Plus and V680 ventilators in the United States due to a potential ...

Murrysville, Pa.-based Philips Respironics Inc. has had its share of troubles with its devices for respiratory use, including several CPAP machines. The FDA reported March 21 that the company’s V60 ...

Royal Philips (NYSE: PHG) (AEX: PHIA), a global leader in health technology, today announced the Philips V60 Plus ventilator has received CE mark approval. This comprehensive solution expands on ...

Amsterdam, the Netherlands – Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, today announced that its subsidiary Philips Respironics is notifying customers of its V60/V60 ...

Philips V60 Plus ventilator receives CE Mark, expands on Philips' commitment and leadership in hospital respiratory care New comprehensive solution enhances clinician workflow and maximizes equipment ...