Home / Brands / Epilog Laser

Epilog Laser Recalls

1 recall on record · December 11, 2024 to December 11, 2024 · Medical Devices

December 11, 2024Medical DevicesFDA

Epilog Laser Corp. recalls Fusion Pro 24, Model 17000

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.

Epilog Laser Recalls | RecallWatchUSA