Class II

Medical Device Recall: Material Processing Laser Products

SHENZHEN ATOMSTACK TECHNOLOGIES · September 30, 2025

Reason for Recall

Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3)

Distribution

U.S.

Quantity Affected

N/A

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0888-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.