# FDA recall Z-2525-2024

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2024-07-02.

## Product

Luminos Agile Max -Intended to visualize anatomical structures by converting an x-ray pattern into a visible image.  Model Number: 10762472

## Reason for recall

The support arm may unintentionally lower resulting in injury to persons when they are under the  display ceiling/wall suspension when positioning the displays

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2525-2024
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-07-02
- **Report date:** 2024-08-14

- **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-2525-2024

## Citation

> AI Analytics. FDA recall Z-2525-2024. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2525-2024. Source: US FDA. Licensed CC0.

---

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