FDA Issues Highest-Level Recall for CPAP Machines After Defect Found That Can Shut Them Off During Sleep

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

Federal Regulators Classify a Sleep Apnea Machine Firmware Recall as Class I After 196 Units Went Uncorrected

MedPAC's chair defended its $76 billion Medicare Advantage estimate at an insurer event. What the fight could mean for Part B premiums. Kennedy Disclosure Shows $4 Million in Book Advances From ...
KERO-TV

Following initial recall, reworked sleep apnea machines are recalled

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 ...

Austin judge questions Philips investors' bid for whistleblower records in CPAP recall

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