# FDA recall Z-2149-2025

> **Jinan Bodor Cnc Machine Co Ltd** · Class II · device recall initiated 2025-02-07.

## Product

Bodor's I series laser cutting machine.

## Reason for recall

The Bodor i Series products fail to meet certain applicable Federal standards, 21 CFR 1040.10(f)(1) and 21 CFR 1040.10(f)(2).

## Distribution

US

## Key facts

- **Recall number:** Z-2149-2025
- **Recalling firm:** Jinan Bodor Cnc Machine Co Ltd
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-07
- **Report date:** 2025-07-30

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Jinan, N/A, China

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2149-2025

## Citation

> AI Analytics. FDA recall Z-2149-2025. Retrieved 2026-07-17 from https://api.ai-analytics.org/recall/Z-2149-2025. Source: US FDA. Licensed CC0.

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