---
title: "Spectral CT on Rails, Software Version Number 5.1.0, Model number: 728334; — FDA record Z-1324-2025 | Is It on Recall"
description: "Multiple problems identified with the software version leading to various scanning and image issues, and unintended device movement."
url: https://isitonrecall.com/recall/fda-device-z-1324-2025-spectral-ct-on-rails-software-version-number-5-1-0-model-number-728334/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Spectral CT on Rails, Software Version Number 5.1.0, Model number: 728334; — FDA record Z-1324-2025

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 Feb 28, 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**: Spectral CT on Rails, Software Version Number 5.1.0, Model number: 728334;
- **Reason**: Multiple problems identified with the software version leading to various scanning and image issues, and unintended device movement.
- **Classification**: Class II
- **Recalling firm**: Philips Medical Systems Nederland B.V.
- **Quantity**: 1 unit
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1324-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1324-2025%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 | Software Version Number 5.1.0; Model number: 728334; UDI-DI: (01)00884838103627(21)1005; Serial Number (SN): 1005; |

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

## Distribution

Domestic: MN

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

- [Minnesota](https://isitonrecall.com/state/minnesota/)

## Dates in the source

- **Report date**: Mar 19, 2025
- **Recall initiation date**: Feb 28, 2025
- **Center classification date**: Mar 12, 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-1324-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. records](https://isitonrecall.com/brand/philips-medical-systems-nederland-b-v/)