Z-0768-2025 Class II Ongoing
FDA device recall Z-0768-2025 was initiated by Jinan Bodor Cnc Machine Co Ltd on December 19, 2024 and is designated Class II. Reason for recall: Non-compliant laser products The recall status is ongoing. Affected quantity: 269 units.
Recall Details
- Product Type
- Devices
- Report Date
- January 29, 2025
- Initiation Date
- December 19, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- FDA Mandated
- Product Quantity
- 269 units
Product Description
Bodor P and C series laser cutting machines
Reason for Recall
Non-compliant laser products
Distribution Pattern
US Nationwide Distribution
Code Information
P series is 2421537-000 and C series is 2421612-000.