Reported Aug 20, 2025 · Ongoing
DreamStation Auto CPAP. Non-Continuous Ventilator.
Philips Respironics, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Philips Respironics, Inc. · 1001 Murry Ridge Ln · Murrysville, PA · 15668-8517
Is this the product you have?
- DreamStation Auto CPAP. Non-Continuous Ventilator.
- Lot codes and dates
- Model No. UDSX500S11F
- UDI
606959429765Serial No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
- Amount recalled
- 57 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
Stop using this product now
Devices may possess a programming error resulting in an incorrect device configuration.
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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