Recall archive / FDA device enforcement
Bodor's I series laser cutting machine. — FDA record Z-2149-2025
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Feb 7, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Bodor's I series laser cutting machine.
- Reason
- 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).
- Classification
- Class II
- Recalling firm
- Jinan Bodor Cnc Machine Co Ltd
- Quantity
- 20
- Agency-reported status
- Ongoing
- Source record identifier
- Z-2149-2025
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | The Accession Number is 2421628- 001. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Jul 30, 2025
- Recall initiation date
- Feb 7, 2025
- Center classification date
- Jul 23, 2025
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.