FDA DevicesClass II
Material Processing Laser Products
Published: January 7, 2026Recall ID: Z-0888-2026Category: devicesCountry: US
Medical DeviceFDA Devices
US
Material Processing Laser Products
Recalling Firm: SHENZHEN ATOMSTACK TECHNOLOGIES
Reason for Recall / Hazard
Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3)
Product Description & Identification
Material Processing Laser Products
Additional Source Details
| Field | Value |
|---|---|
| City | Guangdong |
| State | N/A |
| Event id | 98118 |
| Address 1 | 3 Baolong 6 Rd |
| Address 2 | N/A |
| Code info | N/A |
| Postal code | N/A |
| Report date | 20260107 |
| Product type | Devices |
| Product quantity | N/A |
| Reason for recall | Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3) |
| Voluntary mandated | FDA Mandated |
| Recall initiation date | 20250930 |
| Initial firm notification | N/A |
| Center classification date | 20251231 |
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Overview
- Recalling FirmSHENZHEN ATOMSTACK TECHNOLOGIES
- StatusOngoing
- Risk LevelClass II
- DistributionU.S.
Recall Hazard Severity
Official Agency AlertHigh Alert (Class I)
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🚨 SAFETY ALERT: SHENZHEN ATOMSTACK TECHNOLOGIES - Material Processing Laser Products Check if your household is affected: https://therecallfile.com/recalls/material-processing-laser-products/FDA-Z-0888-2026
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