# FDA recall Z-1175-2026

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2025-12-29.

## Product

Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T;  Siemens Material Number (SMN): 11574003;  With Software Version VB10D-SP02

## Reason for recall

Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a previous patient may be processed.

## Distribution

Worldwide - US Nationwide distribution in the states of AK, CA, IL, MN, NY, OR, VA, WI and the countries of Austria, Belgium, Denmark, France, Germany, Greece, Ireland, Italy, Netherlands, Norway, South Africa, Spain, Sweden, Switzerland.

## Key facts

- **Recall number:** Z-1175-2026
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-12-29
- **Report date:** 2026-02-04

- **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-1175-2026

## Citation

> AI Analytics. FDA recall Z-1175-2026. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-1175-2026. Source: US FDA. Licensed CC0.

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