Epilog Laser Corp.: Medical Device Recall in 2024 - (Recall #: Z-0524-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Fusion Pro 24, Model 17000

Product Classification:

Class II

Date Initiated: August 8, 2024

Date Posted: December 11, 2024

Recall Number: Z-0524-2025

Event ID: 95757

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 751

Code Information:

Model 17000 Product Report Accession Number: 2021046-000

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

FDA Mandated