Philips Respironics recalls Trilogy Evo, Garbin Evo, and Aeris EVO models with specific serial numbers due to potential environmental debris accumulation causing inaccurate pressure delivery, which could lead to patient harm if not addressed by a care provider.
Environmental debris may accumulate on the internal machine flow sensor causing partial occlusion which may impact accurate delivery of pressure, volume, or flow. A malfunction caused by this issue can result in patient harm up to hypoxemia if not addressed by the care provider.
Philips Respironics is recalling Trilogy Evo, Garbin Evo, and Aeris EVO ventilators with certain model numbers and serial numbers. Environmental debris can accumulate inside the machine's flow sensor, causing partial blockage that may lead to inaccurate pressure, volume, or flow delivery. If not corrected by a healthcare provider, this could result in patient harm such as hypoxemia.
Environmental debris can build up inside the internal machine flow sensor, causing partial occlusion. This may lead to inaccurate delivery of pressure, volume, or flow. If not addressed by a healthcare provider, it can result in patient harm such as hypoxemia.
Patients using these specific ventilator models with the listed serial numbers and model numbers are most at risk. Healthcare providers who use these devices should check if their equipment is affected.
Check if your ventilator has model numbers DS2110X11B, IN2110X15B, JP2110X16B, AU2110X15B, LA2110X15B, or other listed model numbers. Also check the serial numbers provided in the recall notice.
Identify your ventilator model number and serial number to see if it matches the recalled items listed in the notice.
If your device is affected, contact your healthcare provider to determine if they need to address the issue with the device.
The affected models are Trilogy Evo, Garbin Evo, and Aeris EVO with specific model numbers: DS2110X11B, IN2110X15B, JP2110X16B, AU2110X15B, LA2110X15B, and others listed in the recall notice.
Environmental debris can accumulate inside the internal machine flow sensor, causing partial blockage. This may lead to inaccurate delivery of pressure, volume, or flow, which could result in patient harm such as hypoxemia if not addressed by a healthcare provider.
No, you do not need to stop using the device immediately. However, if your device is affected, contact your healthcare provider to determine if they need to address the issue with the device.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-1649-2023 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1649-2023 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.
