Philips has unveiled and received European CE Mark approval for a new non-invasive ventilator, the V60 Plus, that features high flow therapy. Typically high flow therapy is not available in a ...

Philips Respironics, the U.S.-based health care company owned by Dutch technology firm Philips, has recalled a selection of its V60 ventilator devices due to a risk of "receiving reduced oxygen." The ...

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 ...

Philips Respironics is warning customers that some of its ventilators may stop working properly, leaving a patient without respiratory assistance. According to a notice posted Monday by the U.S. Food ...

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 Plus and V680 ventilators ...

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 ...

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 ...

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.

Please provide your email address to receive an email when new articles are posted on . The FDA designated recalls of ventilation products from Hamilton Medical and Philips Respironics. No injuries or ...