← FDA ENFORCEMENT
Z-0888-2026Class II
SHENZHEN ATOMSTACK TECHNOLOGIES
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Recalling firm
SHENZHEN ATOMSTACK TECHNOLOGIES
Product type
Device
Status
Ongoing
Report date
2026-01-07
Distribution
U.S.
Firm state
N/A
Product quantity
N/A
Initiated by
FDA Mandated
Reason for recall
Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3)
Product description
Material Processing Laser Products
Code / lot info
N/A
Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →