The U.S. Food and Drug Administration has announced a Class I recall involving the BMC Medical Luna G3 APAP, model LG3600. Class I is the agency’s most serious recall classification, indicating that ...

WASHINGTON (AP) — The company behind a global recall of sleep apnea machines said Monday it will stop selling the devices in the U.S., under a tentative agreement with regulators that could cost the ...

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 ...

Medical device company Philips announced a recall of millions of sleep apnea machines and ventilators because a material used inside them could put users at risk of cancer or other health issues.

A federal judge in Austin wants to know why a group of international investors is in Texas fighting for documents and testimony from an Austin-area doctor while the group is fighting for the same ...

The U.S. Food and Drug Administration (FDA) announced a recall on approximately 20,160 medical devices used to treat sleep apnea. This is due to a firmware defect. The device recalled is the Luna G3 ...