Several Philips ventilators, CPAP and BiPAP machines were recalled in June 2021. The company is currently working to repair and replace the affected devices.

More than 17 million masks for BiPAP and CPAP machines have been recalled, according to the U.S. Food and Drug Administration.

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.

17M Philips CPAP, BiPAP masks recalled over ‘serious safety concern’ The FDA said a “serious safety concern” with magnets prompted the recall.

Several Philips ventilators, CPAP and BiPAP machines were recalled in June 2021. The company is currently working to repair and replace the affected devices.

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.

Several Philips ventilators, CPAP and BiPAP machines were recalled in June 2021. The company is currently working to repair and replace the affected devices.

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.

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.