Medical device recalls Moderate risk

Jinan Bodor Cnc Machine Co Ltd recalls Bodor P and C series laser cutting machines

Recall date
December 19, 2024
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0768-2025
FDA classification
Class II
Brand / firm
Jinan Bodor Cnc Machine Co Ltd
Sold / distributed
US Nationwide Distribution

Why it was recalled

Non-compliant laser products

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Bodor P and C series laser cutting machines

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