# FDA recall Z-1495-2021

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2021-03-26.

## Product

Artis zee ceiling-interventional Fluoroscopic X-Ray System  Model Number: 10094137

## Reason for recall

Some Artis zee ceiling systems show an increased abrasion of the cabling at the cable outlet of the inner C-arm, the limited functionality may not be sufficient to continue with treatment as planned. This may result in a situation where it is necessary to cancel clinical treatment or to continue treatment on an alternative system.

## Distribution

Nationwide

## Key facts

- **Recall number:** Z-1495-2021
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-03-26
- **Report date:** 2021-05-05

- **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-1495-2021

## Citation

> AI Analytics. FDA recall Z-1495-2021. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-1495-2021. Source: US FDA. Licensed CC0.

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