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Philips Respironics has issued another ventilator recall deemed the most serious type by the FDA as it may cause serious injury or death.
Philips Respironics has removed certain DreamStation devices due to programming errors that can result in failed therapy modes, according to the U.S. Food and Drug Administration.
AMSTERDAM, NETHERLANDS (WTEN0) – Philips Respironics has issued a recall on thousands of ventilators and CPAP machines. The recall only affects units sold in the United States. The units affected ...
LOS ANGELES (KABC) -- Rather than weight loss and surgery, getting a CPAP machine has been the top go-to treatment for people with a severe snoring disorder called sleep apnea. But after the Food and ...
Paris prosecutors opened a criminal probe into Philips in June over its recall of sleep apnea devices, probing possible ...
Loud snoring at night. Pauses in breathing followed by gasps for air while you’re asleep. Excessive daytime fatigue. Frequent nodding off in front of the TV or even when behind the wheel of a car.
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