Philips Respironics recalls Trilogy Evo ventilators with software version 1.05.15.00 due to potential tidal volume discrepancies when used with non-pneumatic nebulizers. Affected units may not deliver correct breathing support.
Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.
Philips Respironics is recalling its Trilogy Evo continuous home ventilators with software version 1.05.15.00 because using non-pneumatic nebulizers can cause incorrect breathing support. This could lead to improper treatment if the ventilator doesn't match the set tidal volume.
The ventilator may not deliver the correct amount of air per breath when paired with non-pneumatic nebulizers, causing the set tidal volume to differ from what the patient actually receives. This could lead to inadequate breathing support if the discrepancy is significant.
People using Philips Respironics Trilogy Evo ventilators with software version 1.05.15.00 at home are affected. Those who use non-pneumatic nebulizers with these devices are at higher risk.
Check for the software version 1.05.15.00 on your Trilogy Evo ventilator. All models, serial numbers, and unique device identifiers are affected.
Verify your ventilator's software version is 1.05.15.00 to confirm if it's affected.
Yes, all Trilogy Evo ventilators with software version 1.05.15.00 are affected.
The recall does not specify a remedy, so you should check the software version and contact Philips Respironics for guidance.
Using non-pneumatic nebulizers with this software version may cause incorrect breathing support, but the recall does not specify serious injury risks.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-1614-2026 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1614-2026 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.
