(WKBN) – The U.S. Food and Drug Administration issued a safety alert on Tuesday about an “emerging safety issue” with some CPAP machines. According to the FDA, the Philips Respironics’ DreamStation 2 ...
Certain Philips Respironics DreamStation breathing devices, commonly used for treating sleep apnea, may deliver the incorrect prescription or no therapy at all, the FDA warned in a recall announcement ...
The FDA said that it has received reports that the machines can overheat and cause “thermal issues such as fire, smoke, burns and other signs of overheating while people are using” the devices. The ...
A voluntary recall of millions of CPAP breathing machines, used mainly to treat sleep apnea, has many users wondering if they've been inhaling cancer-causing toxins in their sleep. At least 25 million ...
“My heart just fell from my chest,” Frank Reese said. It’s been three months since Frank Reese from Bridgeport first learned that his Philips CPAP machine had been recalled. Stream Connecticut News ...
Orlando, Florida — Carrie Markham spent three years struggling to breathe, suffering from lung problems that began in March of 2020, puzzling her doctors. "They just kept saying, 'We just don't know,' ...
The U.S. Food and Drug Administration on Friday announced the recall of certain Philips Respironics devices designed to help people with breathing conditions keep breathing at a regular rhythm. The ...
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