# FDA recall Z-1900-2019

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2019-06-06.

## Product

Siemens Artis Q biplane---Interventional Fluoroscopic X-Ray System  Model Number: 10848282

## Reason for recall

Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed connection joining the pivot bearing to the ceiling-mounted support to work loose or snap off,  can result in severe injuries to patients and operating personnel

## Distribution

Nationwide

## Key facts

- **Recall number:** Z-1900-2019
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-06-06
- **Report date:** 2019-07-10
- **Termination date:** 2021-02-09

- **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-1900-2019

## Citation

> AI Analytics. FDA recall Z-1900-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1900-2019. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*