Shenzhen Atomstack Technologies recalls material processing laser products due to missing remote interlock connector, which may cause safety hazards. Affected units require immediate action.
Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3)
Shenzhen Atom: 1. Shenzhen Atomstack Technologies recalls material processing laser products because they lack a required remote interlock connector. This could lead to safety issues if the laser is used without proper safety mechanisms.
The missing remote interlock connector is required by federal regulations (21 CFR 1040.10(f)(3)) to prevent unsafe operation. Without this connector, the laser could malfunction, potentially causing injury or damage.
Users of material processing laser products from Shenzhen Atomstack Technologies are affected. Those using the products without the required remote interlock connector are at risk.
Check if your material processing laser product has a remote interlock connector as required by 21 CFR 1040.10(f)(3). The product name is listed as 'Material Processing Laser Products' in the recall.
Verify if your material processing laser product has the required remote interlock connector.
The product lacks a required remote interlock connector as specified by federal regulations (21 CFR 1040.10(f)(3)).
The recall record does not specify a remedy, so check the product details to see if it has the required remote interlock connector.
The recall record does not specify a deadline for action.
We’ve drafted a message you can send Shenzhen Atomstack Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-0888-2026 — Shenzhen Atomstack Technologies Shenzhen Atomstack Technologies Hello, I own a Shenzhen Atomstack Technologies that is covered by recall Z-0888-2026 from Shenzhen Atomstack Technologies. 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.
