Class II
Medical Device Recall: Bodor P and C series laser cutting machines
Jinan Bodor Cnc Machine Co Ltd · December 19, 2024
Reason for Recall
Non-compliant laser products
Distribution
US Nationwide Distribution
States Affected
NATIONWIDE
Quantity Affected
269 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0768-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.