There is a risk of serious injury or death related to more than 20 million CPAP masks made by ResMed, the FDA said Jan. 11. The continuous positive airway pressure masks, branded as AirFit and ...
Liran Oren, Ph.D., (left) is shown with Ephraim Gutmark, Ph.D., and Ann Romaker, MD, and the VortexPAP device. Nearly 40 million Americans have obstructive sleep apnea, according to the Council on ...
Just a few weeks after racking up its fifth Class I recall from the FDA this year, Philips has hit the half-dozen mark. Its sixth of the classifications—which denote the agency’s most serious rating ...
Please provide your email address to receive an email when new articles are posted on . The FDA has granted de novo clearance to SoClean 3+, an over-the-counter bacterial reduction device for certain ...
Thousands of people with sleep apnea and other illnesses had sued the company, claiming flawed devices were harming them. By Christina Jewett Philips Respironics has reached a $1.1 billion settlement ...
WASHINGTON - A massive recall of millions of sleep apnea machines has stoked anger and frustration among patients, and U.S. officials are weighing unprecedented legal action to speed up a replacement ...
In late November, ResMed issued a safety notice warning that some of the masks used with its CPAP machines contain magnets that could potentially interfere with pacemakers, neurostimulators and other ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results