Bodor recalls I series laser cutting machines for failing to meet federal safety standards. Affected units may pose risks if not properly maintained.
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).
Bodor is recalling its I series laser cutting machines because they don't meet federal safety standards. This could lead to safety risks if the machines aren: t properly maintained.
The machines fail to meet federal safety standards, which could result in safety hazards if not properly maintained. Without meeting these standards, the machines might not function safely under normal use conditions.
Users of Bodor's I series laser cutting machines are affected. Those operating these machines in industrial settings are most at risk.
Check for the Bodor I series laser cutting machines. The Accession Number for this recall is 2421628-001.
Identify if your machine is part of the I series with Accession Number 2421628-001.
The Bodor I series laser cutting machines fail to meet certain federal safety standards, which could pose safety risks if not properly maintained.
The recall record does not specify a remedy, so check with the manufacturer for next steps.
The recall mentions the Accession Number 2421628-001, but no specific model or serial numbers are provided.
We’ve drafted a message you can send Bodor to request your refund or repair — edit it as you like.
Subject: Recall Z-2149-2025 — Bodor Bodor Hello, I own a Bodor that is covered by recall Z-2149-2025 from Bodor. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
