# FDA recall Z-2129-2024

> **Rygel Advanced Machines d/b/a Omtech Laser** · Class II · device recall initiated 2024-06-07.

## Product

OMTech Desktop Laser Engraver

## Reason for recall

Lack of redundant interlocks, missing required labels and certification labels as required by 21 1010.2.

## Distribution

US Nationwide

## Key facts

- **Recall number:** Z-2129-2024
- **Recalling firm:** Rygel Advanced Machines d/b/a Omtech Laser
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-07
- **Report date:** 2024-06-19

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Anaheim, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2129-2024

## Citation

> AI Analytics. FDA recall Z-2129-2024. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2129-2024. Source: US FDA. Licensed CC0.

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