Reworked DreamStation Recall

April 7, 2023 Philips DreamStations Recall - The United States Food & Drug Administration (FDA) has issued a notice that certain Philips Respironics DreamStation CPAP and BiPAP machines have been recalled. This recall is for certain reworked DreamStation devices that were assigned incorrect or duplicate serial numbers. A machine with an incorrect serial number is a problem because therapy may be delivered using the wrong prescription or factory default settings. It could even fail to deliver any therapy. If such an error occurs, there is no warning or alert. This failure could lead to health problems such as respiratory failure, heart failure, injury, or death.

For questions and support, please contact Philips Respironics by calling 1-877-387-3311 or by emailing patientsupport@philips.com. You can also visit the FDA website to learn more.