Philips sent updated instructions related to a problem with bilevel positive airway pressure, or BiPAP, machines that can cause interruption or loss of therapy. Philips recalled three models of BiPAP ...
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 ...
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 ...
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 ...
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, ...
The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines. A Class I recall means the FDA has ...
Electronics manufacturing giant Philips is recalling millions of CPAP and BiPAP devices due to an issue that could potentially pose a health risk to users of the machines. In the wake of the recall, ...
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 ...
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