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 ...

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 ...

Respironics is recalling the V60 Non-invasive Ventilator because the pins within the internal cable that connects the ventilator’s motor to the control board may become loose over time due to low ...

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 ...

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 ...

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 ...

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 ...

May 22 (Reuters) - U.S. FDA: * Respironics California recalls the V60 non-invasive ventilator due to faulty cable pins that may cause the device to shut down unexpectedly Sign up here. * Respironics ...

Respironics California Inc is recalling 19,200 V60 ventilators worldwide because of a serious safety issue with the software on the device's power management board assembly. If a component fails on ...

Philips Respironics has recalled some ventilators meant to provide breathing support after four injuries and one death have been attributed to the devices. According to an announcement with the U.S.