Bodor Laser Cutting Machines Recall: Non-Compliant Laser Products

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Recalling firmJinan Bodor Cnc Machine Co LtdNO.1299, XINLUO AVE HI-TECH ZONE · Jinan, N/A

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Bodor P and C series laser cutting machines are being recalled because they do not meet safety standards. This could pose a risk of injury from improper laser operation.

Why it’s dangerous

The machines are non-compliant with safety standards, which may lead to improper laser operation. This could result in potential injuries if the laser is used without proper safety measures.

Who’s affected

Users of Bodor P and C series laser cutting machines, particularly those in industrial or manufacturing settings, are most at risk.

How to tell if you have this one

Check for the model numbers: P series is 2421537-000 and C series is 2421612-000. These machines were sold by Jinan Bodor Cnc Machine Co Ltd.

Brand
Bodor
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Model Number
Identify the model number on your machine to confirm if it is a recalled P series (2421537-000) or C series (2421612-000).

✎ GovInfoNow

Questions people ask

What models are affected by this recall?

The affected models are Bodor P series (2421537-000) and C series (2421612-000).

How can I tell if my machine is recalled?

Check the model number on your machine; if it matches P series 2421537-000 or C series 2421612-000, it is affected.

What should I do if I have a recalled machine?

The recall record does not specify a remedy, so contact the manufacturer for further instructions.

Take action

Contact Bodor

We’ve drafted a message you can send Bodor to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0768-2025 — Bodor Bodor

Hello,

I own a Bodor that is covered by recall Z-0768-2025 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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Where this comes from

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.

Official source: FDA Recall #Z-0768-2025 (December 19, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0768-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

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

Recall notice