# FDA recall Z-2302-2020

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2020-04-30.

## Product

Multi Display Manager in the Artis Systems (Image-Intensified Fluoroscopic X-Ray System)  as follows:    Artis Q floor     Model: 10848280;   Artis Q ceiling  Model: 10848281;  Artis Q biplane  Model:10848282;   Artis zee ceiling Model: 10094137;   Artis zee floor     Model: 10094135     Product Usage: Artis is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.

## Reason for recall

Artis systems containing a Multi Display Manager of a specific lot, the power distributor may lead to an increased electrical contact resistance or the interruption of electrical contact, and result in planned procedures to be terminated and performed on an alternative x-ray system

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2302-2020
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-04-30
- **Report date:** 2020-06-17
- **Termination date:** 2020-09-11

- **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-2302-2020

## Citation

> AI Analytics. FDA recall Z-2302-2020. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-2302-2020. Source: US FDA. Licensed CC0.

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