# FDA recall Z-1000-2023

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2022-12-09.

## Product

AXIOM Luminos TF, AXIOM Iconos R100, AXIOM Iconos R200 and AXIOM Luminos dRF

## Reason for recall

There is potential for the footrest to detach from the patient table during use.

## Distribution

Worldwide distribution

## Key facts

- **Recall number:** Z-1000-2023
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-12-09
- **Report date:** 2023-01-25

- **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-1000-2023

## Citation

> AI Analytics. FDA recall Z-1000-2023. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-1000-2023. Source: US FDA. Licensed CC0.

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