Philips DreamStation Auto BiPAP and CPAP: Cloud Connection Issues May Affect Settings
Philips recalls limited DreamStation Auto BiPAP and CPAP units with model numbers UCDSX500S11, UDSX500S11, etc. for potential cloud communication issues that could cause incorrect prescription settings or inability to download settings. Affected units may need verification.
Lower-risk recall
A limited number of remediated Philips DreamStation units may experience communication issues when connecting to the cloud-based care management application. Should this be the case, this may affect the ability to download prescription settings to the device or the device may have incorrect prescription settings for the patient.
Contact the company
What happened, in plain English
Philips is recalling certain DreamStation Auto BiPAP and CPAP machines that may have communication problems with their cloud-based care management app. This could lead to incorrect prescription settings or the device not being able to download settings. Users should check if their device is affected. Read more at govinfonow.com/recall/58914-philips-dreamstation-auto-bipap-and-cpap-cloud-connection-issues-may.
Source Summary by GovInfoNow · govinfonow.com/recall/58914-philips-dreamstation-auto-bipap-and-cpap-cloud-connection-issues-may · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1322-2023
Cite this page
“Philips DreamStation Auto BiPAP and CPAP: Cloud Connection Issues May Affect Settings.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/58914-philips-dreamstation-auto-bipap-and-cpap-cloud-connection-issues-may. Based on FDA recall #Z-1322-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1322-2023%22&limit=1).
Why it’s dangerous
The device may experience communication issues with the cloud-based care management application, which could result in incorrect prescription settings being applied or the device not being able to download prescription settings from the cloud. This is a communication issue, not a physical hazard.
Who’s affected
People who own or use Philips DreamStation Auto BiPAP or CPAP machines with the listed model numbers and serial numbers are most at risk. This recall affects a limited number of units.
How to tell if you have this one
Check if your device has model numbers UCDSX500S11, UDSX500S11, UDSX500S11F, UDSX700S11, or UDSX700S11F. Also, verify your serial number is in the list provided in the recall notice.
- Brand
Philips- Category
Medical device
What to do — step by step
Check Device Model
Identify your DreamStation device model number to see if it matches the recalled models listed in the recall notice.
Verify Serial Number
Check if your device's serial number is in the list of affected serial numbers provided in the recall notice.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “US Nationwide. France, Reunion.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1322-2023 (February 10, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1322-2023 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.