HME News

Philips removes certain DreamStation devices

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.
MassDevice

FDA updates on serious Philips CPAP, BiPAP device recall

Philips Respironics has issued another ventilator recall deemed the most serious type by the FDA as it may cause serious injury or death.
Healio

FDA designates Philips Respironics DreamStation recall as class I

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 ...
CNN

Some Philips CPAP, BiPAP machines may not work as intended, FDA says in recall

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 ...