the most serious type of recall," the agency said Friday in issuing a new alert about the the devices. The repaired CPAP machines were given the wrong or a duplicate serial number when Philips re ...

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 ...

More than two years after the recall, Don Schreiber of Pleasant Hills finally got a replacement machine. When he got his new CPAP, he checked the serial number and found that it, too, was on the ...

The FDA announced that recalled CPAP and BiPAP machines have been ... search the serial number here to find out if it’s part of the recall. If you have a recalled device, the FDA urges patients ...

In a statement posted on the Food and Drug Administration's website, Phillips says the machines were assigned duplicate or incorrect serial ... SEE MORE: Recall of Philips CPAP device causing ...

An online reviewer is warning about a CPAP machine recall. He claims The Philips Dreamstation ... cancer risk are picking up a significant number of views on TikTok. Nicko posted the video warning ...

CPAP machines made by Philips NV are the subject of a recall and various lawsuits by people who allege they were harmed by them. The number of lawsuits filed over the CPAP devices is so large that ...

People who have bought, leased or rented certain Philips Respironics sleep apnea machines can now file a claim for restitution. The Dutch medical equipment maker recently agreed to pay at least $ ...