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 ...

Please provide your email address to receive an email when new articles are posted on . The FDA designated the recall of Philips Respironics DreamStation devices as class I. The devices are used in ...

Please provide your email address to receive an email when new articles are posted on . Philips Respironics will stop selling its sleep therapy and respiratory care devices in the U.S. until it meets ...

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 ...