Quick Facts at a Glance
- Recall Date
- September 30, 2025
- Hazard Level
- HIGH
- Brand
- SHENZHEN ATOMSTACK TECHNOLOGIES
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- SHENZHEN ATOMSTACK TECHNOLOGIES
- Product type
- Material Processing Laser Products
- Sold at
- Multiple Retailers
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
September 30, 2025
Reported by FDA DEVICE
January 7, 2026
RecallRadar source check
January 14, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3)
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact SHENZHEN ATOMSTACK TECHNOLOGIES or your healthcare provider for instructions. Notification method: N/A
About This Product
Material processing laser products are used in various industrial and medical applications for precise cutting and engraving. Consumers purchase these devices for efficiency in material handling and processing tasks.
Why This Is Dangerous
The absence of a remote interlock connector means the device can operate without safety measures in place, potentially leading to accidents or injuries.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers must stop using these devices immediately, leading to potential disruptions in operations that utilize these lasers.
Practical Guidance
How to identify if yours is affected
- Check if you own any material processing laser products from SHENZHEN ATOMSTACK TECHNOLOGIES.
- If unsure, stop using the product until you verify its status with the manufacturer.
- Review any documentation or packaging for model details.
Where to find product info
Typically, the model number can be found on the product label or within the user manual.
What timeline to expect
Expect a timeline of 4-6 weeks for refund processing after the recall instructions are followed.
If the manufacturer is unresponsive
- Document all communication attempts with the manufacturer.
- Consider reaching out to consumer protection agencies for assistance.
How to prevent similar issues
- Ensure future purchases include verified safety features such as remote interlock connectors.
- Look for products with clear compliance with safety regulations.
Documentation advice
Keep records of your purchase, any communication with the manufacturer, and photographs of the product.
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Product Details
The recall involves material processing laser products from SHENZHEN ATOMSTACK TECHNOLOGIES. These devices were distributed in the U.S. The specific model numbers are not available.
Key Facts
- Recall date: September 30, 2025
- Manufacturer: SHENZHEN ATOMSTACK TECHNOLOGIES
- Lack of remote interlock connector
- Class II medical device recall
- Immediate stop-use advisory
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Safety Guide
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