Class II
Medical Device Recall: Bodor's I series laser cutting machine.
Jinan Bodor Cnc Machine Co Ltd · February 7, 2025
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).
Distribution
US
Quantity Affected
20
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2149-2025
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.