Philips Respironics recalls Trilogy EV300 ventilators with specific model numbers due to potential aerosol buildup causing inaccurate flow measurements. Affected users should check their model numbers and contact Philips for details.
Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.
Philips Respironics is recalling specific models of Trilogy EV300 ventilators because aerosol deposits on the internal flow sensor can cause inaccurate flow measurements. This could lead to improper treatment settings for patients using the device.
In certain locations, aerosol deposits can accumulate on the device's internal flow sensor. This accumulation may cause inaccurate flow measurements, potentially leading to improper treatment settings for patients.
Users of Trilogy EV300 ventilators with model numbers DS2200X11B, IN2200X15B, BL2200X15B, BR2200X18B, CA2200X12B, DE2200X13B, GB2200X15B, and other listed models. Patients using these ventilators for medical ventilation are most at risk.
Check the model number on your Trilogy EV300 ventilator. The affected models include DS2200X11B, IN2200X15B, BL2200X15B, BR2200X18B, CA2200X12B, DE2200X13B, GB2200X15B, and other listed models. All serial numbers are affected.
Identify your Trilogy EV300 model number to confirm if it is affected.
The affected models include DS2200X11B, IN2200X15B, BL2200X15B, BR2200X18B, CA2200X12B, DE2200X13B, GB2200X15B, and other listed models.
The recall is due to potential aerosol deposit accumulation on the internal flow sensor, which could lead to inaccurate flow measurements.
If your model number is not listed, it is not affected by this recall.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0293-2025 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-0293-2025 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.
