# FDA recall Z-2529-2025

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2025-08-12.

## Product

Artis Pheno. Image-Intensified Flouroscopic X-Ray System.

## Reason for recall

Limited system movements after startup .

## Distribution

US Nationwide distribution in the states of AL, AZ, FL, KY, MA, MI, NY, OR, A, TN, TX & UT.

## Key facts

- **Recall number:** Z-2529-2025
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-08-12
- **Report date:** 2025-09-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Malvern, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2529-2025

## Citation

> AI Analytics. FDA recall Z-2529-2025. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-2529-2025. Source: US FDA. Licensed CC0.

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