Bodor's I series laser cutting machine recall
Bodor's I series laser cutting machine.
Why was Bodor's I series laser cutting machine 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).
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
The Accession Number is 2421628- 001.
- Product
- Bodor's I series laser cutting machine.
- Recalling firm
- Jinan Bodor Cnc Machine Co Ltd
- Quantity
- 20
- Distribution
- US
- Recall date
- July 30, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)