Bodor P and C series laser cutting machines — FDA record Z-0768-2025

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 Dec 19, 2024. 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 P and C series laser cutting machines
Reason
Non-compliant laser products
Classification
Class II
Recalling firm
Jinan Bodor Cnc Machine Co Ltd
Quantity
269 units
Agency-reported status
Ongoing
Source record identifier
Z-0768-2025

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityP series is 2421537-000 and C series is 2421612-000.

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

US Nationwide Distribution

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Jan 29, 2025
Recall initiation date
Dec 19, 2024
Center classification date
Jan 18, 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.

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