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.

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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 ...

Philips Respironics has promised to replace millions of CPAP and BiPAP breathing machines that FDA reports have linked to thousands of injuries and more than 300 deaths.More than two years after the ...

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, ...

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 ...

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 ...

FROM SHADYSIDE TONIGHT. PHILIPS REIS RUN ROAD RECALLED MILLIONS OF CPAPS BIPAPS AND VENTILATORS AFTER THE FDA SAID FOAM INSULATION INSIDE THOSE MACHINES WAS A HEALTH RISK. BUT IN A LAWSUIT, PHILIPS ...

New York City-based Northwell Health said it has developed a protocol to transform a BiPAP machine into a functional ventilator and that it plans to share the design online so other hospitals facing ...

NEW HYDE PARK, N.Y.--(BUSINESS WIRE)--In preparation for potential patient surge and shortage of critical mechanical ventilators for hospitalized COVID-19 patients, a Northwell Health physician, a ...