FDA Device recall Z-1290-2023
GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Light Show (LLS)projectors for the purposes of demonstration and entertain…
- FDA Device
- Class II
- ongoing
- Published 2023-04-05
On 2023-04-05 the FDA classified a Class II recall of GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Light Show (LLS)projectors for the purposes of demonstration and entertain… by Gaga Pro Lighting Equipment, citing GAGA Pro LLS systems was not in compliance with the FDA's Performance Standard for laser products.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1290-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-09-23 |
| Published | 2023-04-05 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Gaga Pro Lighting Equipment |
| Distribution | US |
Product
GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Light Show (LLS)projectors for the purposes of demonstration and entertainment.
Reason
GAGA Pro LLS systems was not in compliance with the FDA's Performance Standard for laser products.
Identifiers
| code_info | GA-RGB3000, GA-A4-W10000, GA-ML500-8, GA-RGB8000, GA-RGB4000, GA-RGB5000, GA-G4000M, and GA-ML1800 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1290-2023%22
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