Philips Respironics recalls DreamStation Auto BiPAP non-continuous ventilators with a programming error that could cause incorrect device configuration. Affected models include UDSX70:11F and specific serial numbers. Contact for remedy.
Devices may possess a programming error resulting in an incorrect device configuration.
Philips Respironics is recalling DreamStation Auto BiPAP non-continuous ventilators due to a programming error that might cause incorrect device settings. This could affect users who rely on the device for breathing support.
The device may have a programming error that leads to incorrect configuration settings. This could potentially cause the ventilator to function improperly, but the risk is not described as causing serious injury in normal use.
People using DreamStation Auto BiPAP non-continuous ventilators for breathing support are most at risk. The recall affects specific model numbers and serial numbers listed in the notice.
Check for model number UDSX700S11F and specific serial numbers listed in the recall notice. The product is sold under Philips Respironics.
Verify if the device configuration matches the manufacturer's specifications.
The recall states a programming error could cause incorrect device configuration, but it does not describe a risk of serious injury in normal use.
The recall does not specify a remedy, so contact Philips Respironics directly for guidance.
Affected models include UDSX700S11F with specific serial numbers listed in the recall notice.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-2228-2025 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-2228-2025 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.
