# FDA recall Z-0726-2018

> **NeuroLogica Corporation** · Class II · device recall initiated 2017-06-22.

## Product

The GC80 Digital X-ray Imaging System

## Reason for recall

An image was obtained with over exposure during a Thorax examination using the AEC function.

## Distribution

Nationwide US

## Key facts

- **Recall number:** Z-0726-2018
- **Recalling firm:** NeuroLogica Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-22
- **Report date:** 2018-03-14
- **Termination date:** 2018-10-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Danvers, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0726-2018

## Citation

> AI Analytics. FDA recall Z-0726-2018. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-0726-2018. Source: US FDA. Licensed CC0.

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