Vaccines.gov's ZIP code search is not working as flu season starts. Here is how to find flu, COVID, and RSV shots at pharmacies and health centers. Sandoz will pay $400 million to settle state claims ...

The Food and Drug Administration has classified a firmware defect in 20,160 BMC Medical sleep apnea machines as a Class 1 ...

A defective firmware update could cause certain Luna G3 APAP machines to shut down unexpectedly, interrupting therapy while users are asleep.

Koninklijke Philips NV has filed a third-party complaint in Pennsylvania federal court against SoClean Inc., which sells cleaning products for breathing devices, claiming SoClean and its parent should ...

Phillips has recalled more than 1,000 reworked Respironics DreamStation CPAP, BiPAP machines. The machines, initially recalled in June 2021, may still not be working correctly. In a statement posted ...

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.

Over 20,000 machines are impacted by this recall. The FDA recalled 20,160 Luna G3 APAP machines due to a firmware defect. The recall is classified as Class I, meaning the defect could lead to serious ...

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 ...