Philips Respironics recalls Trilogy Evo Universal Ventilators (model DS2000X11B) due to potential inaccurate flow measurements from aerosol deposits. Affected units may require servicing to prevent incorrect ventilation 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 its Trilogy Evo Universal Ventilators (model DS2000X11B) because aerosol deposits can cause inaccurate flow measurements. This could lead to improper ventilation settings for patients, especially in critical care situations.
Aerosol deposits can build up in the device's internal flow sensor, causing inaccurate flow measurements. This might lead to incorrect ventilation settings for patients, potentially affecting treatment effectiveness.
Patients using the Trilogy Evo ventilator for medical ventilation, particularly those in hospitals or home care settings. Healthcare providers and caregivers responsible for the device are most at risk.
The Trilogy Evo Universal Ventilator with model number DS2000X11B. All units sold with serial numbers are affected. This device is used for medical ventilation in institutional, home, and non-emergency transport settings.
Verify the model number on your ventilator; affected units have DS2000X11B.
Reach out to Philips Respironics for guidance on next steps.
The recall is due to potential aerosol deposits causing inaccurate flow measurements, which could affect ventilation settings.
Check the model number; if it's DS2000X11B, contact Philips Respironics for guidance.
The recall addresses potential inaccurate flow measurements, not immediate injury risks. The hazard level is low risk.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0292-2025 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-0292-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
