Philips Respironics recalls Trilogy Evo ventilators (all software versions except 1.05.06.00) due to potential sudden loss of ventilation when battery or power alarms trigger without actual power loss.
Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
Philips Respironics is recalling all Trilogy Evo ventilators except those with software version 1.05.06.00. The device may lose ventilation unexpectedly if battery or power alarms sound even when the unit still has power.
The ventilator may show battery or power alarms while still having sufficient power. This can cause sudden loss of ventilation, meaning the device stops supporting breathing without warning.
Pediatric and adult patients using the Trilogy Evo ventilator are affected. Patients with breathing support needs are most at risk.
Check for model numbers starting with AU, BL, BR, CA, DE, DS, EE, ES, EU, FR, FX, GB, IA, IN, IT, JP, KR, LA, LD, ND, RDS, SP, TR, UDS, or VT. All units except those with software version 1.05.06.00 are affected.
Look for the software version on the device label or documentation; if it's 1.05.06.00, this unit is not affected.
If the device shows battery or power alarms but still has power, stop using it immediately to prevent sudden loss of ventilation.
All Trilogy Evo ventilators except those with software version 1.05.06.00. Model numbers start with AU, BL, BR, CA, DE, DS, EE, ES, EU, FR, FX, GB, IA, IN, IT, JP, KR, LA, LD, ND, RDS, SP, TR, UDS, or VT.
The recall does not specify a fix; users should stop using the device if alarms trigger without actual power loss.
Check the model number on the device or documentation. Affected units have model numbers starting with AU, BL, BR, CA, DE, DS, EE, ES, EU, FR, FX, GB, IA, IN, IT, JP, KR, LA, LD, ND, RDS, SP, TR, UDS, or VT, and software versions other than 1.05.06.00.
We’ve drafted a message you can send Philips Respironics to request your refund or repair — edit it as you like.
Subject: Recall Z-1504-2024 — Philips Respironics Philips Respironics Hello, I own a Philips Respironics that is covered by recall Z-1504-2024 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.
