# FDA recall Z-0721-2020

> **Mazor Robotics Ltd** · Class II · device recall initiated 2019-07-02.

## Product

Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868

## Reason for recall

The firm  has become aware that the Snapshot Trackers were not manufactured in accordance with specifications and could potentially lead to navigational inaccuracies, which may result in patient injury, e.g. nerve damage or neurological deficit/dysfunction

## Distribution

US: Arizona, Arkansas, California, Colorado, Connecticut, Florida, Georgia, Illinois, Indiana, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, New York, North Carolina, North Dakota, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, West Virginia

## Key facts

- **Recall number:** Z-0721-2020
- **Recalling firm:** Mazor Robotics Ltd
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-07-02
- **Report date:** 2020-01-01
- **Termination date:** 2022-02-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Caesarea, Israel

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0721-2020

## Citation

> AI Analytics. FDA recall Z-0721-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0721-2020. Source: US FDA. Licensed CC0.

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