Epilog Laser

1 recall Categories: Other Medical Devices
Class I - Dangerous

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.

Aug 8, 2024 Other Medical Devices Nationwide View Details →