Fusion Pro 24, Model 17000

This recall is currently active, issued December 3, 2024. It was issued by Epilog Laser Corp..

Company

Epilog Laser Corp.

Recall Initiated

August 8, 2024

Posted

December 3, 2024

Recall Number

Z-0524-2025

Quantity

751

Firm Location

Golden, CO

Official Source

View on FDA website ↗

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

Lot / Code Info

Model 17000 Product Report Accession Number: 2021046-000

Root Cause

Radiation Control for Health and Safety Act

Action Taken

The measures to be taken to repair such defect or to bring the product into compliance with the Federal standard. This Recall provides corrections by repair to a defective safety interlock location by a kit with comprehensive instructions, offered at no cost to purchasers