The risk assessments have now been completed for the CPAP/BiPAP sleep therapy devices under the recall notification/field safety notice* i.e., the first-generation DreamStation, System One and DreamStation Go devices, representing approximately 95% of the registered devices globally. The assessments build on the previous updates in
The test and research program has been conducted together with five independent, certified testing laboratories, and the results have been reviewed and assessed by third-party qualified experts and
The full press release is available here.
* Voluntary recall notification in the US/field safety notice for the rest of the world.
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Philips Global Press Office
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Attachment
- Philips provides update on completed set of test results for cpap bipap sleep therapy devices
Source: Royal Philips
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