Reported Aug 20, 2025 · Ongoing
DreamStation Auto BiPAP. 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 BiPAP. Non-Continuous Ventilator.
- Lot codes and dates
- Model No. UDSX700S11F
- UDI
606959429772Serial No. J18909076CC90J2091514323C5J2164570462CBJ23391208BCBEJ26552747A030J2909781691D2J294724447698J301490021E77
- Amount recalled
- 8 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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