Bodor P and C series laser cutting machines
FDA Recall #Z-0768-2025 — Class II — December 19, 2024
Product Description
Bodor P and C series laser cutting machines
Reason for Recall
Non-compliant laser products
Recalling Firm
Jinan Bodor Cnc Machine Co Ltd — Jinan
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
269 units
Distribution
US Nationwide Distribution
Code Information
P series is 2421537-000 and C series is 2421612-000.
Status
Ongoing
Voluntary / Mandated
FDA Mandated