Philips Respironics recalls Trilogy Evo Universal Ventilators (Model DS2000X11B) for potential safety issues in pediatric patients. Affected units have specific serial numbers; users should stop using and contact Philips for details.
The Trilogy Evo Universal ventilator provides continuous or intermittent positive pressure ventilation for the care of individuals who require mechanical ventilation. Trilogy Evo Universal is intended for pediatric through adult patients weighing at least 2.5 kg. The ventilator can measure, display, record, and alarm SpO2, FiO2, CO2, and pulse rate data when integrated with the appropriate accessories. The ventilator is suitable for use in institutional and hospital settings and non-emergency transport settings; for example, wheelchair. It may be used for both invasive and non-invasive ventilation.
Philips Respironics is recalling its Trilogy Evo Universal Ventilators (Model DS2000X11B) due to potential safety risks for pediatric patients. This device is used for mechanical ventilation in children and adults weighing at least 2.5 kg. The recall does not specify a hazard mechanism but lists affected serial numbers.
The recall does not specify a hazard mechanism or risk description. The product is intended for mechanical ventilation in patients who require it, but the official notice does not explain why this model is being recalled.
Pediatric patients and adults weighing at least 2.5 kg who use the Trilogy Evo Universal Ventilator for mechanical ventilation. The recall affects specific units with the listed serial numbers.
Check if your ventilator has the model number DS2000X11B and the listed serial numbers (e.g., H27736231F4BE, H277362379188, etc.). The recall includes specific serial numbers provided in the record.
Verify if your ventilator has the model number DS2000X11B and one of the listed serial numbers (e.g., H27736231F4BE, H277362379188, etc.).
The recall does not specify a hazard mechanism or risk description. The official notice lists affected units but does not explain why this model is being recalled.
Check if your ventilator has the model number DS2000X11B and one of the listed serial numbers. If it does, stop using it and contact Philips Respironics for further instructions.
The recall does not specify a hazard mechanism or risk description. The official notice does not indicate a specific injury 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-1652-2023 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1652-2023 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.
