Philips Respironics recalls Garbin Evo ventilators (model LD2110X23B) due to potential inaccurate flow measurements from aerosol deposits. Affected units may require cleaning or adjustment to ensure proper ventilation.
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 Garbin Evo ventilators (model LD2110X23B) 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 certain locations inside the ventilator's flow sensor. This may cause the device to give incorrect flow readings, potentially leading to improper ventilation settings for patients.
Patients using the Garbin Evo ventilator for breathing support in hospitals, clinics, or home care settings. Those with the model number LD2110X23B are most at risk.
Check for the model number LD2110X23B on the device or its packaging. The ventilator is intended for use with patients weighing at least 2.5 kg in institutional, home, or non-emergency transport settings.
Look for the model number LD2110X23B on the device or its packaging.
The recall is due to potential aerosol deposits in certain locations that could cause inaccurate flow measurements, which might lead to improper ventilation settings.
Check the model number on the device or packaging. If it matches LD2110X23B, contact Philips Respironics for guidance on cleaning or adjustments.
The hazard is low risk as it involves potential inaccuracies in flow measurements rather than immediate physical danger.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-0295-2025 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-0295-2025 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.
