# FDA recall Z-1878-2025

> **Flux Technology Inc.** · Class II · device recall initiated 2025-02-19.

## Product

Lazervida 10W diode laser cutter and engraver with Lazervida shield.

## Reason for recall

Lazervida 10W Diode Laser Engraver does not fully meet current Federal performance standards  in certain areas. Specifically, the product does not incorporate the additional beam  attenuator, remote interlock connector, key switch, specific labels and manual instructions  required under current regulations.

## Distribution

US

## Key facts

- **Recall number:** Z-1878-2025
- **Recalling firm:** Flux Technology Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-19
- **Report date:** 2025-06-11

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Taipei City, N/A, Taiwan

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1878-2025

## Citation

> AI Analytics. FDA recall Z-1878-2025. Retrieved 2026-08-23 from https://api.ai-analytics.org/recall/Z-1878-2025. Source: US FDA. Licensed CC0.

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