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Epilog Laser Corp.
1 federal recall on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Epilog Laser Corp. and translate it into plain English — free weekly digest, optional same-day alerts.
- 2024-12-11FDA-DeviceClass IIFusion Pro 24, Model 17000
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.
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