Jinan Bodor Cnc Machine Co Ltd: Device Recall

Recall #Z-0768-2025 · 12/19/2024

Class II: Risk

Recall Details

Recall Number: Z-0768-2025
Classification: Class II
Product Type: Device
Recalling Firm: Jinan Bodor Cnc Machine Co Ltd
Status: Ongoing
Date Initiated: 12/19/2024
Location: Jinan, China
Voluntary/Mandated: FDA Mandated
Product Quantity: 269 units

Reason for Recall

Non-compliant laser products

Product Description

Bodor P and C series laser cutting machines

Distribution Pattern

US Nationwide Distribution

Other Recalls by Jinan Bodor Cnc Machine Co Ltd

Class II: Risk 02/07/2025

The Bodor i Series products fail to meet certain applicable Federal standards, 21 CFR 1040.10(f)(1) and 21 CFR 1040.10(f)(2).

View all recalls by Jinan Bodor Cnc Machine Co Ltd →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.