The agency, in a statement issued last week, said it has received more than 116,000 reports about the breathing devices — BiPAP and CPAP machines — over nearly three years.

Now, Philips is recalling another 1,200 reworked CPAP and BiPAP devices that it says may fail to deliver the correct respiratory therapy—or any treatment at all.

Nearly two years after Philips first publicly raised concerns about the potential breakdown of the polyester-based polyurethane foam found in many of its CPAP and BiPAP machines and other ...

It researched, developed, designed, manufactured, sold, distributed and marketed CPAP machines, as well as other devices aimed at treating respiratory failure and breathing disorders such as BiPAP ...

The agency, in a statement issued last week, said it has received more than 116,000 reports about the breathing devices — BiPAP and CPAP machines — over nearly three years.