Ongoing Class II Medical devices
- Recall started
- 30 September 2025
- Reason
- Lack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3)
- Distribution
- U.S.
- Initiated
- FDA Mandated
- Recall number
- Z-0888-2026
- Material Processing Laser Products
Guangdong, N/A, China
1 recall recorded since 2018, most recently on 30 September 2025. 1 is listed as ongoing. Status and classification are as published by the FDA.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.