# FDA recall Z-2746-2017

> **Medtronic Navigation, Inc.** · Class II · device recall initiated 2017-05-10.

## Product

Install CD, Spine tools, Plus and S7, Version 25.  Model Number 9731958.

## Reason for recall

Software issue related to the StealthStation S7 system and the Synergy Spine application Version 2.1 configured with Spine Tool Install CD version 25.  Issue may result in user being unable to navigate the Navigated Elevate Inserter with the StealthAiR Spine Frame during spine surgical procedures.

## Distribution

Worldwide Distribution - USA (nationwide) Distribution and to the countries of :  Brazil, Germany, Switzerland and Great Britain.

## Key facts

- **Recall number:** Z-2746-2017
- **Recalling firm:** Medtronic Navigation, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-10
- **Report date:** 2017-07-26
- **Termination date:** 2021-01-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Louisville, CO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2746-2017

## Citation

> AI Analytics. FDA recall Z-2746-2017. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2746-2017. Source: US FDA. Licensed CC0.

---

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