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Epilog Laser Corp. recalls Fusion Pro 24, Model 17000
Recalled December 11, 2024 · FDA recall Z-0524-2025 · Epilog Laser
Hazard
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. · FDA Class II
Units
751
Sold at
US Nationwide Distribution
Description
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.
Product
Fusion Pro 24, Model 17000
Manufacturer(s)
Epilog Laser Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →