Jinan Bodor Cnc Machine Co Ltd recalls Bodor's I series laser cutting machine.
- Recall date
- February 7, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2149-2025
- FDA classification
- Class II
- Brand / firm
- Jinan Bodor Cnc Machine Co Ltd
- Sold / distributed
- US
Why it was recalled
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).
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's I series laser cutting machine.
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