# FDA recall Z-1056-2024

> **NeuroLogica Corporation** · Class II · device recall initiated 2023-12-28.

## Product

Samsung Digital Diagnostic Mobile X-ray System, Model GM85.

## Reason for recall

Mobile x-ray systems moving arm frame welding issue which presents the potential of bodily harm due to fall of the arm.

## Distribution

US Nationwide Distribution including states of: AL, AR, CA, CO, CT, DC, FL, GA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OK, PA, SD, TN, TX, VA, WI & WV.

## Key facts

- **Recall number:** Z-1056-2024
- **Recalling firm:** NeuroLogica Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-12-28
- **Report date:** 2024-02-21

- **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-1056-2024

## Citation

> AI Analytics. FDA recall Z-1056-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1056-2024. Source: US FDA. Licensed CC0.

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