SHENZHEN ATOMSTACK TECHNOLOGIES recalls Material Processing Laser Products
Reason for recall
Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3)
Affected product
Material Processing Laser Products
What the firm is doing
CAP letter to be sent to customers.
DistributionShow detailsHide
U.S.
Use of the product may cause temporary or medically reversible adverse health consequences.
Sources & references
- FDA enforcement recordOfficial FDA database entry for Z-0888-2026
- FDA device classification · RFEOfficial FDA classification for this device type
- FDA recall announcementSearch FDA.gov for the official press announcement
- Find SHENZHEN ATOMSTACK TECHNOLOGIESSearch for the manufacturer's official notice
- News coverageRecent reporting on this recall and manufacturer
- openFDA data recordThe raw JSON record this page is built from
Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.
Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.
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