HIGH

SHENZHEN ATOMSTACK TECHNOLOGIES Recalls Laser Products Over Safety Hazard

SHENZHEN ATOMSTACK TECHNOLOGIES recalled material processing laser products on September 30, 2025, due to a missing remote interlock connector. This defect poses a high risk according to federal regulations. Consumers should stop using these devices immediately and follow manufacturer instructions for remedy.

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

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

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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.

The Hazard

The material processing laser products lack a remote interlock connector, which is required by 21 CFR 1040.10(f)(3). This connector is essential for safe operation and to prevent accidents.

Reported Incidents

No specific incidents or injuries have been reported regarding this recall. The absence of the required connector presents a high risk of safety hazards.

What to Do

Stop using the devices immediately. Contact SHENZHEN ATOMSTACK TECHNOLOGIES or your healthcare provider for further instructions regarding the recall.

Contact Information

For more information, visit the FDA recall page at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=Z-0888-2026.

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 Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeMaterial Processing Laser Products
Sold At
Multiple Retailers

Product Details

Report Date
January 7, 2026
Recall Status
ACTIVE

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