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The Philips recall covers a broad range of devices. The DreamStation series — including DreamStation CPAP, Auto CPAP, BiPAP, DreamStation Go, DreamStation ASV, and DreamStation ST/AVAPS — is the most common recalled product line and represents the majority of plaintiff devices in MDL 3014. The System One 50 and 60 Series (CPAP, Auto CPAP, BiPAP, ASV, ST variants) are the primary legacy product line. Additional recalled models include the REMstar SE Auto CPAP, Dorma 400 and 500 CPAPs, OmniLab Advanced+ titration device, A-Series BiPAP A30 and A40, and Trilogy 100 and 200 life-sustaining ventilators.
If you used a Philips Respironics CPAP or BiPAP device and are unsure whether your model is recalled, check the model number on the device label against the FDA recall list or contact us for a free verification. The recall registration website (set up by Philips) is another resource, but registration does not release your legal claims. Keep your device — it is physical evidence.
The full investigation