Per the Philips Respironics recall notice:

Per Philips Respironics CEO Frans van Houten “We deeply regret any concern and inconvenience that patients using the affected devices will experience because of the proactive measures we are announcing today to ensure patient safety.” On Monday, June 14th, Philips Respironics issued a voluntary recall on nearly all of their CPAP, APAP, and BiPAP machines sold from 2009 until today, with some exceptions. As information becomes available, we will update our customers via email and the CPAP community at large using this blog. Not all details of this recall are known at this time. We will continue to take any actions Philips Respironics or the organizations governing them approve relating to this recall as quickly as we are able to execute them.īelow is the information you need to know on this recall, how you might be impacted, what next steps should be taken, and what you should expect. We have completed all requests by Philips Respironics and we eagerly await a plan that will allow us to provide actionable solutions to customers. We learned of this recall at the same time as our customers and have been in daily communication with Philips Respironics since that time.ĭespite sincere and full efforts by members of the Philips Respironics team we’ve been in contact with, details and actions we can take immediately to have a positive impact on the health of our customers have been in short supply. All of the relationships we hold dear, our family, friends, coworkers, and customers are affected.

Since the news broke, customers have let us know they are frustrated and concerned. was recently notified by Philips Respironics of a recall for certain CPAP, APAP, and BiPAP devices.

Philips dreamstation recall