# FDA recall Z-0956-2023

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

## Product

ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor

## Reason for recall

Mechanical connection between the tabletop and table base may be lost.

## Distribution

Worldwide distribution - US Nationwide and the countries of Armenia, Australia, Austria, Belgium, Bulgaria, Canada, Chile, China, Colombia, Czech Republic, Denmark, Egypt, Finland, France, Germany, Greece, Hong Kong, India, Indonesia, Iran, Ireland, Italy, Japan, Kazakhstan, Kuwait, Lebanon, Monaco, Netherlands, New Zealand, Norway, Oman, Poland, Qatar, Russian Federation, Saudi Arabia, Singapore, Slovakia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, United Arab Emirates, United Kingdom, and Vietnam.

## Key facts

- **Recall number:** Z-0956-2023
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-12-16
- **Report date:** 2023-01-25

- **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-0956-2023

## Citation

> AI Analytics. FDA recall Z-0956-2023. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-0956-2023. Source: US FDA. Licensed CC0.

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