# FDA recall Z-0695-2020

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2019-11-14.

## Product

Artis zee/ zeego Interventional Fluoroscopic X-Ray System, Model Number: 10094142, Software Version: VC21C

## Reason for recall

In affected Artis zee floor Interventional Fluoroscopic X-Ray Systems, the activation of a collision sensor will cause a block the movement of the floating tabletop and could result in a delay or interruption of a procedure.

## Distribution

US: WA and TX  International: Denmark

## Key facts

- **Recall number:** Z-0695-2020
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-11-14
- **Report date:** 2019-12-25
- **Termination date:** 2020-05-12

- **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-0695-2020

## Citation

> AI Analytics. FDA recall Z-0695-2020. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-0695-2020. Source: US FDA. Licensed CC0.

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