Jinan Bodor Cnc Machine Co Ltd: Device Recall
Recall #Z-2149-2025 · 02/07/2025
Class II: Risk
Recall Details
- Recall Number
- Z-2149-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Jinan Bodor Cnc Machine Co Ltd
- Status
- Ongoing
- Date Initiated
- 02/07/2025
- Location
- Jinan, N/A, China
- Voluntary/Mandated
- FDA Mandated
- Product Quantity
- 20
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).
Product Description
Bodor's I series laser cutting machine.
Distribution Pattern
US
Other Recalls by Jinan Bodor Cnc Machine Co Ltd
- Class II: Risk 12/19/2024
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.