Philips Respironics recalls Aeris EVO ventilators (model VT2110X24B) due to potential inaccurate flow measurements from aerosol deposits. Affected units sold to patients weighing at least 2.5 kg in institutional or home settings.
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 Aeris EVO ventilators (model VT2110X24B) because aerosol buildup in certain locations can cause inaccurate flow measurements. This could lead to improper treatment settings for patients using the device.
Aerosol deposits can accumulate on the device's internal flow sensor in specific locations, causing the ventilator to give inaccurate flow measurements. This might lead to improper treatment settings if the device is used without proper calibration.
Patients weighing at least 2.5 kg using the Aeris EVO ventilator in institutional, home, or non-emergency transport settings. Healthcare providers and caregivers responsible for these patients are most at risk.
Check for model number VT2110X24B on the device or its packaging. The ventilator is intended for patients weighing at least 2.5 kg in institutional, home, or non-emergency transport settings.
Look for model number VT2110X24B on the device or its packaging.
The recall is due to potential aerosol deposits on the internal flow sensor causing inaccurate flow measurements, which could lead to improper treatment settings.
Patients weighing at least 2.5 kg using the Aeris EVO ventilator in institutional, home, or non-emergency transport settings.
Check the model number on the device or packaging. If it matches VT2110X24B, contact Philips Respironics for guidance.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0294-2025 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-0294-2025 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.
