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.

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.

Philips released the latest set of safety test results (PDF) on Tuesday, covering all of the CPAP and BiPAP sleep therapy machines included in the recall—which together make up about 95% of all ...

In 2021, polyester-based polyurethane (PE-PUR) foam used in Philips Respironics ventilators, CPAP and BiPAP machines were found to degrade and cause serious health issues or death, leading to a ...

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.