# FDA recall Z-1040-2023

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2022-12-16.

## Product

System	Material #  Artis zee floor 	10094135  Artis zee ceiling 	10094137  Artis zee multi-purpose	10094139  Artis zee biplane	10094141  Artis zeego	10280959  Artis Q floor	10848280  Artis Q ceiling	10848281  Artis Q biplane	10848282  Artis Q.zeego	10848283  Artis Q.zen floor	10848353  Artis Q.zen ceiling	10848354  Artis Q.zen biplane	10848355        Fluoroscopic X-Ray System

## Reason for recall

In rare cases, the system may only boot into backup mode after an abrupt shutdown and not reach full operating mode.  This may result in a situation where it is necessary to cancel clinical treatment or to continue treatment on an alternative system.

## Distribution

Worldwide - US Nationwide distribution.

## Key facts

- **Recall number:** Z-1040-2023
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-12-16
- **Report date:** 2023-02-08

- **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-1040-2023

## Citation

> AI Analytics. FDA recall Z-1040-2023. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1040-2023. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*