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Open, Classified

Material Processing Laser Products

FDA Recall Z-0888-2026 · Posted 2025-12-31

Recalling FirmSHENZHEN ATOMSTACK TECHNOLOGIES
Recall StatusOpen, Classified
Product CodeRFE
Date Initiated2025-09-30

Reason for Recall

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

Firm Action

CAP letter to be sent to customers.

Root Cause

Radiation Control for Health and Safety Act

Distribution Pattern

U.S.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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