FDA Medical Device Recalls (openFDA)
GAGA PRO LIGHTING EQUIPMENT CO.,: GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Light Show (LLS)projectors for the purposes of demonstration and entertainment.
- Recall number
- Z-1290-2023
- Recalling firm
- GAGA PRO LIGHTING EQUIPMENT CO.,
- Product
- GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Light Show (LLS)projectors for the purposes of demonstration and entertainment.
- Status
- Open, Classified
- Initiated
- 2022-09-23
- Posted
- 2023-03-29
- Terminated
- not on file
- Reason
- GAGA Pro LLS systems was not in compliance with the FDA's Performance Standard for laser products.
- Root cause
- Radiation Control for Health and Safety Act
- Action
- GaGa. will send a Customer Notification letter to the affected customers by certified mail. The letter will identify the affected product, problem and actions to be taken. GAGA lighting will offer free upgrades to update your GAGA Laser projector to the current FDA requirements. Alternatively, you may choose to ship your laser projector to GAGA Lighting s U.S. agent, Laser Display Company, in order to get it fixed. GAGA Lighting will pay for shipping costs. GAGA Lighting, without charge, will bring the product into compliance with each applicable Federal standard for laser products.
- Quantity
- 11 units
- Distribution
- US Nationwide Distribution
- Lot, serial or model codes
- GA-RGB3000, GA-A4-W10000, GA-ML500-8, GA-RGB8000, GA-RGB4000, GA-RGB5000, GA-G4000M, and GA-ML1800
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- REA
- Firm FEI
- 3013936259
- Firm city
- Guangzhou
- Firm state
- Area
- Firm country
- China
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28