Philips Respironics recalls Trilogy Evo O2 ventilators with specific model numbers due to potential aerosol buildup causing inaccurate flow measurements. Affected units may need adjustment to prevent incorrect readings.
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 Evo O2 ventilators because aerosol deposits can accumulate on internal sensors, leading to inaccurate flow measurements. This could cause incorrect treatment settings for patients using the device.
The device's internal flow sensor can accumulate aerosol deposits in certain locations, which may cause inaccurate flow measurements. This could lead to incorrect ventilation settings for patients, potentially affecting treatment effectiveness.
Patients using the Trilogy Evo O2 ventilators with model numbers listed in the recall are affected. Healthcare providers and caregivers responsible for these devices are most at risk of incorrect treatment settings.
Check the model number on your Trilogy Evo O2 ventilator. Affected models include FP2100X10, DS2100X11B, IN2100X15B, DE2100X13B, IA2100X15B, EU2100X15B, LA2100X15B, and others listed in the recall notice.
Identify your Trilogy Evo O2 ventilator's model number to confirm if it is affected by this recall.
The recall is due to potential aerosol deposit accumulation on the internal flow sensor, which could cause inaccurate flow measurements in certain locations.
Affected models include FP2100X10, DS2100X11B, IN2100X15B, DE2100X13B, IA2100X15B, EU2100X15B, LA2100X15B, and others listed in the recall notice.
The recall does not require immediate action, but you should check your model number to see if it is affected. If affected, contact Philips Respironics for further instructions.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0290-2025 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-0290-2025 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.
