FDAFebruary 7, 2025device

Bodor's I series laser cutting machine.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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).

What to do

FDA enforcement status: Ongoing

Brands named

jinan bodor cnc machinejinanjinan bodor

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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