Philips Respironics recalls LifeVent EVO2 ventilators (model SP2100X26B) due to potential aerosol buildup causing inaccurate flow readings. Affected units may require correction to avoid incorrect ventilation 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 LifeVent EVO2 ventilators (model SP2100X26B) because aerosol deposits can cause inaccurate flow measurements. This could lead to improper ventilation settings if not corrected, especially in medical use.
Aerosol deposits can accumulate in the device's internal flow sensor, causing it to measure airflow incorrectly. This might lead to improper ventilation settings if the device is not properly maintained or calibrated.
Patients using LifeVent EVO2 ventilators for medical ventilation, particularly those in institutional or home care settings. Healthcare providers and caregivers are most at risk of incorrect treatment due to inaccurate flow readings.
Check for model number SP2100X26B on the device. The product is intended for medical use in institutions, homes, and non-emergency transport settings for patients weighing at least 2.5 kg.
Look for model number SP2100X26B on the device label or documentation.
The recall is due to potential aerosol buildup in the device's flow sensor that could cause inaccurate flow measurements, which might lead to improper ventilation settings.
The hazard is low risk as it involves potential inaccuracies in flow measurements rather than immediate safety risks like fire or injury.
Check for model number SP2100X26B on the device. The product is intended for medical use in institutions, homes, and non-emergency transport settings for patients weighing at least 2.5 kg.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0296-2025 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-0296-2025 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.
