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Open, Classified

Bodor's I series laser cutting machine.

FDA Recall Z-2149-2025 · Posted 2025-07-23

Recalling FirmJinan Bodor Cnc Machine Co Ltd
Recall StatusOpen, Classified
Product CodeRFE
Date Initiated2025-02-07
Product Quantity20

Reason for Recall

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).

Firm Action

Jinan Bodor CNC Machine Co. Ltd., and its subsidiary, Bodor Laser Inc., (collectively and individually, Bodor ) sent letters to customers to inform them the FDA has determined that i Series Products fail to meet certain applicable Federal Standards. The letter also provides Corrective Action Plan and instructions of 'Continued Use of Product While Corrective Actions are Pending'.

Root Cause

Radiation Control for Health and Safety Act

Distribution Pattern

US

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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