Recall Z-0888-2026— SHENZHEN ATOMSTACK TECHNOLOGIES
Class II · Ongoing
Class II FDA medical device recall by SHENZHEN ATOMSTACK TECHNOLOGIES, initiated 2025-09-30. FDA's recall record names no specific 510(k) clearance for this event. Product: Material Processing Laser Products. Reason: Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3).
- Recalling firm
- SHENZHEN ATOMSTACK TECHNOLOGIES
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-09-30
- Firm location
- Guangdong, N/A, China
Product description
Material Processing Laser Products
Reason for recall
Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3)
Data sourced from openFDA. This site is unofficial and independent of the FDA.