# FDA recall Z-2715-2024

> **NeuroLogica Corporation** · Class II · device recall initiated 2024-07-08.

## Product

GM60A. Digital Diagnostic Mobile X-Ray System.

## Reason for recall

Potential for the anti-fall system of the device arm to fail.

## Distribution

US Nationwide distribution in the states of AR, CT, GA, IN, KS, MA, MD, MO, MS, NC, ND, NJ, NV, OH, PA, VA, WV & DC.

## Key facts

- **Recall number:** Z-2715-2024
- **Recalling firm:** NeuroLogica Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-07-08
- **Report date:** 2024-08-28

- **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-2715-2024

## Citation

> AI Analytics. FDA recall Z-2715-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2715-2024. Source: US FDA. Licensed CC0.

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