Z-0888-2026Class II

Material Processing Laser Products

Name: Z-0888-2026 Material Processing Laser Products
Creator: Shenzhen Atomstack Technologies
Published: 2025-09-30
License: https://open.fda.gov/license/

Shenzhen Atomstack Technologies / initiated 2025-09-30 / Open, Classified

FDA source

SHENZHEN ATOMSTACK TECHNOLOGIES began a recall of Material Processing Laser Products on 2025-09-30. FDA classified it as Class II and gives the reason as "Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3)". As of 2026-09-10, the recall status on record is Open, Classified.

Recall record

Recall number: Z-0888-2026
Classification: Class II
Status: Open, Classified
Initiated: 2025-09-30
Posted: 2025-12-31
Recalling firm: Shenzhen Atomstack Technologies
Product: Material Processing Laser Products
Product code: RFE Laser Cutter
Reason for recall: Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3)
FDA root cause: Radiation Control for Health and Safety Act
Action: CAP letter to be sent to customers.
Distribution: U.S.
Product codes and lots: N/A

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0888-2026
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0888-2026	Class II	Ongoing	FDA Mandated	2026-01-07	2025-12-31

Product code RFE

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)