They will start selling the DreamStation 2 again when they are close to fulfilling all the registered requests. On 3/23/2022, Philips added a patient portal where you can check your device status here: Philips is asking customers at this time to inform them if they need Prioritization due ...
The FDA has designated Philips Respironics’ recall of DreamStation devices as class I — the most serious kind. The devices were recalled occurred because some were assigned serial numbers that were either incorrect or duplicates during the initial programming, which can cause therapy to be de...
In the US, the recall notification has been classified by the FDA as a Class I recall. [1] This includes DreamStation CPAP, Auto CPAP; Dream Station Bi-Level PAP; DreamStation ASV; and DreamStation ST, AVAPS devices. [2] T...
Since 2021, Philips has been battling a series of crises over its DreamStation machines forsleep apnea, a disorder in which breathing stops and starts during sleep. Users were at risk of inhaling or swallowing pieces of toxic soundproofing foam that could cause irritation or headaches. The US F...