# FDA recall Z-0579-2025

> **Orthoscan, Inc.** · Class II · device recall initiated 2024-08-08.

## Product

Ziehm Vision RFD 3D. Interventinoal fluoroscopic x-ray system

## Reason for recall

Ziehm Imaging, Inc., distributor, have been informed by manufacturer, Ziehm Imaging GmbH that installed devices may not fully meet the requirements of IEC 60601-2-54 and or 21 CFR 1020.32(c) with respect to wired hand switch may fail when being exposed to mechanical stress such as shocks (e.g. dropping) or impacts can irreversibly damage the switching element in the hand switch. A defective switching element may then potentially initiate unintended radiation of the connected mobile X-ray unit.

## Distribution

U.S. (including Puerto Rico).

## Key facts

- **Recall number:** Z-0579-2025
- **Recalling firm:** Orthoscan, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-08-08
- **Report date:** 2024-12-11

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Scottsdale, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0579-2025

## Citation

> AI Analytics. FDA recall Z-0579-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0579-2025. Source: US FDA. Licensed CC0.

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