Over 20,000 machines are impacted by this recall.

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

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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.

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 ...

Attorneys who filed a class action lawsuit against Philips over its now-recalled respiratory devices filed additional court papers on Monday detailing what they called delays in the company’s response ...

Investors seeking evidence for planned Dutch litigation face questions over pursuing the same information in two states.

Add Yahoo as a preferred source to see more of our stories on Google. The FDA recalled 20,160 Luna G3 APAP machines due to a firmware defect. The recall is classified as Class I, meaning the defect ...

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 ...