The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines. A Class I recall means the FDA has ...
Ingrid Tischer needs a machine to sleep. For nearly 30 years, she’s been using BiPAP devices, which push pressurized air into her lungs so she gets enough oxygen through the night. In June, a friend ...
This is an archived article and the information in the article may be outdated. Please look at the time stamp on the story to see when it was last updated. (WKBN) – More than 17 million masks for ...