Philips Respironics recalls DreamStation Auto CPAP devices with a programming error that may cause incorrect device configuration. Affected units include specific model numbers and serials. Consumers should contact Philips for guidance.
Devices may possess a programming error resulting in an incorrect device configuration.
Philips Respironics is recalling DreamStation Auto CPAP devices due to a potential programming error that could lead to incorrect device settings. This issue may affect users who rely on the device for breathing support, as improper settings could disrupt treatment effectiveness.
The devices may have a programming error that results in incorrect device configuration. This could lead to improper treatment settings for users who rely on the CPAP for breathing support. However, the error does not cause immediate harm or injury in normal use.
People using Philips Respironics DreamStation Auto CPAP devices for sleep apnea treatment are most at risk. The recall affects specific model numbers and serials listed in the official notice.
Check the model number (UDSX500S11F) and serial numbers listed in the recall notice. Affected units have specific serial numbers starting with J204432084D03 through J30982199BB1D.
Verify your DreamStation Auto CPAP model number is UDSX500S11F.
Reach out to Philips Respironics for guidance on whether your device is affected and next steps.
The recall is for a potential programming error that could cause incorrect device configuration, but it does not pose an immediate risk of injury or harm in normal use.
Check the model number (UDSX500S11F) and serial numbers listed in the recall notice, which include specific numbers starting with J204432084D03 through J30982199BB1D.
Contact Philips Respironics for guidance on whether your device is affected and next steps.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-2227-2025 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-2227-2025 from Philips Respironics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
