FDA Medical devices recall ·
Material Processing Laser Products recall
- Recall number
- Z-0888-2026
- Date
- (initiated September 30, 2025)
- Company / brand
- Shenzhen Atomstack Technologies
3 Baolong 6 Rd, Guangdong, N/A, China - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- N/A
- Initiated by
- FDA Mandated
Read the official FDA notice ↗
Product
Material Processing Laser Products
Why was it recalled?
Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3)
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
N/A
Distribution
U.S.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-0888-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.