Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Fusion Pro 24 Recalled by Epilog Laser Corp. Due to a. A small number of Fusion Pro 24...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Epilog Laser Corp. directly.
Affected Products
Fusion Pro 24, Model 17000
Quantity: 751
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Epilog Laser Corp.
Epilog Laser Corp. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report