# FDA recall Z-0879-2026

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2025-10-24.

## Product

MAMMOMAT Fusion;

## Reason for recall

There were instances where the operator table was sold together with a bus-installation kit. The operator table is not intended and not released for bus installations as it was designed for stationary operation only.

## Distribution

Worldwide - US Nationwide distribution in the states of AR, CA, NY and the countries of  Australia, Canada, India.

## Key facts

- **Recall number:** Z-0879-2026
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-10-24
- **Report date:** 2025-12-10

- **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-0879-2026

## Citation

> AI Analytics. FDA recall Z-0879-2026. Retrieved 2026-07-17 from https://api.ai-analytics.org/recall/Z-0879-2026. Source: US FDA. Licensed CC0.

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