# FDA recall Z-2643-2026

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2026-05-20.

## Product

ARTIS icono floor. Model Number: 11327700.

## Reason for recall

Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2643-2026
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-20
- **Report date:** 2026-07-08

- **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-2643-2026

## Citation

> MORVS. FDA recall Z-2643-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-2643-2026. Source: US FDA. Licensed CC0.

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