# FDA recall Z-1343-2022

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2022-05-24.

## Product

Artis zeego (Model no.  10280959) and Artis Q.zeego (Model no. 10848283), Interventional Fluoroscopic X-Ray System

## Reason for recall

It may occur that after system startup no stand movement is possible any longer in the event of a discharged BIOS battery of the robotic stand control PC. If this problem occurs during startup, all stand movements are blocked and can only be reactivated by a field service engineer.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of AL, AR, CA, CO, FL,  IL, LA, ME, MN, MO, NC, OH, PA, SC, TN, TX, WI and the countries of Australia, Austria,  Azerbaijan, Belgium, Canada, China, Finland, France, Germany, Hong Kong, India, Italy,  Japan, Lebanon, Lithuania, Luxembourg, Netherlands, Poland, Portugal, South Korea, Switzerland, United Kingdom.

## Key facts

- **Recall number:** Z-1343-2022
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-05-24
- **Report date:** 2022-07-13
- **Termination date:** 2025-01-22

- **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-1343-2022

## Citation

> AI Analytics. FDA recall Z-1343-2022. Retrieved 2026-07-15 from https://api.ai-analytics.org/recall/Z-1343-2022. Source: US FDA. Licensed CC0.

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