# FDA recall Z-1825-2026

> **PHILIPS MEDICAL SYSTEMS** · Class II · device recall initiated 2026-03-07.

## Product

Philips Spectral CT on Rails. Model Number: 728334.

## Reason for recall

Philips has identified three software issues:  1. During a continuous CT (CCT) scan, there is the potential that the Gantry could remain at the current scan position after pressing Go.   2. Potential where the message of Previous Surview Exists Select Previous Surview? <Yes> or <No> should display but does not appear.   3. After performing Surview and planning the Brain Helical acquisition by setting Brain Area DoseRight Index to increase the dose, there is the potential that the Define Head Area option in the context menu is grayed out.

## Distribution

Worldwide - US Nationwide distribution in the states of Minnesota and the countries of France and Netherlands.

## Key facts

- **Recall number:** Z-1825-2026
- **Recalling firm:** PHILIPS MEDICAL SYSTEMS
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-07
- **Report date:** 2026-04-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Cambridge, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1825-2026

## Citation

> AI Analytics. FDA recall Z-1825-2026. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-1825-2026. Source: US FDA. Licensed CC0.

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