---
title: "Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143; — FDA record Z-1794-2025 | Is It on Recall"
description: "Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application."
url: https://isitonrecall.com/recall/fda-device-z-1794-2025-product-name-evolution-upgrade-3-0t-model-numbers-1-782117-2-782143/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143; — FDA record Z-1794-2025

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 May 13, 2025. 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**: Product Name: Evolution Upgrade 3.0T; Model Numbers: (1) 782117, (2) 782143;
- **Reason**: Potential for alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
- **Classification**: Class II
- **Recalling firm**: Philips North America Llc
- **Quantity**: 28 units (5 US, 23 OUS)
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1794-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1794-2025%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 Numbers: (1) 782117, (2) 782143; UDI-DI: (1) 00884838099739, (2) 00884838108660; Serial Numbers: (1) 42023, 42024, 42078, 42375, 42402, 42408, 71348, 85675, 85687, 85694, 85705, (2) 42193, 42225, 42308, 42320, 42366, 42415, 71595, 71815, 71836, 85649, 85684, 85688, 85690, 85695, 85697, 85699, 85708; |

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

## Distribution

Worldwide distribution - US Nationwide and the countries of Andorra, Argentina, Australia, Austria, Belgium, Brazil, Canada, Chile, Colombia, C¿te D'Ivoire, Cyprus, Czech Republic, Denmark, Finland, France, French Guiana, Georgia, Germany, Greece, Guadeloupe, Hong Kong, Iceland, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kenya, Latvia, Lebanon, Libya, Lithuania, Malaysia, Malta, Martinique, Mexico, Moldova, Monaco, Netherlands, New Zealand, Norway, Palestine, Philippines, Poland, Portugal, Qatar, Romania, Russian Fed., Serbia, Slovenia, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Ukraine, United Kingdom, U.A.E.

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

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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: May 28, 2025
- **Recall initiation date**: May 13, 2025
- **Center classification date**: May 16, 2025

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-1794-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Philips North America Llc records](https://isitonrecall.com/brand/philips-north-america-llc/)
