---
title: "Trilogy Evo Universal Ventilator, all software versions except 1.05.06.00. Ve... — FDA record Z-1505-2024 | Is It on Recall"
description: "Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power."
url: https://isitonrecall.com/recall/fda-device-z-1505-2024-trilogy-evo-universal-ventilator-all-software-versions-except-1-05-06-00-ventilator-for-pediatric-an/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Trilogy Evo Universal Ventilator, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients. — FDA record Z-1505-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Mar 19, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Trilogy Evo Universal Ventilator, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.
- **Reason**: Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
- **Classification**: Class I
- **Recalling firm**: Philips Respironics, Inc.
- **Quantity**: 9,999 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1505-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1505-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Model No. DS2000X11B; UDI-DI: 606959052000; All units except those with software version 1.05.06.00. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Domestic: Nationwide Distribution; Foreign: AE, AR, AT, AU, BD, BE, BG, BO, BR, BS, CA, CH, CL, CN, CO, CZ, DE, DK, DZ, EC, EE, EG, ES, FI, FR, GB, GE, GF, GI, GR, GT, HK, HR, HU, ID, IE, IL, IN, IT, JE, JO, JP, KE, KR, KW, LB, LT, MA, ME, MK, MM, MQ, MT, MX, MY, NG, NL, NO, NP, NZ, OM, PA, PE, PF, PH, PK, PL, PR, PT, PY, QA, RE, RO, RS, RU, SA, SE, SG, SI, SK, TH, TN, TR, TW, UA, US, UY, VN, YT, ZA, ZW.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Apr 24, 2024
- **Recall initiation date**: Mar 19, 2024
- **Center classification date**: Apr 17, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1505-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Philips Respironics, Inc. records](https://isitonrecall.com/brand/philips-respironics-inc/)
