# FDA recall Z-0524-2025

> **Epilog Laser Corp.** · Class II · device recall initiated 2024-08-08.

## Product

Fusion Pro 24, Model 17000

## Reason for recall

a. A small number of Fusion Pro 24 units were released with an incorrectly placed Interlock device. As a result, the system can be operated with the front-loading door in an open position.  b. Fails to comply with Class 2 designation, indicated in Part 6 of Laser Product Report. An incorrectly placed Interlock device can allow Class 4 laser radiation fields during operation.

## Distribution

US Nationwide Distribution

## Key facts

- **Recall number:** Z-0524-2025
- **Recalling firm:** Epilog Laser Corp.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-08-08
- **Report date:** 2024-12-11

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Golden, CO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0524-2025

## Citation

> AI Analytics. FDA recall Z-0524-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-0524-2025. Source: US FDA. Licensed CC0.

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