GaGa Pro Lighting Equipment Co — Class II medical device recall Z-1290-2023
Ongoing recall by GAGA PRO LIGHTING EQUIPMENT CO.,, reported 2023-04-05, distributed nationwide. GAGA Pro LLS systems was not in compliance with the FDA's Performance Standard for laser products.
| Recall number | Z-1290-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | FDA mandated |
| Recalling firm | GAGA PRO LIGHTING EQUIPMENT CO.,, Guangzhou, N/A, China |
| Recall initiated | 2022-09-23 |
| Classified | 2023-03-29 |
| Reported by FDA | 2023-04-05 |
| Distributed | Nationwide (US) |
| Quantity | 11 units |
Product
GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Light Show (LLS)projectors for the purposes of demonstration and entertainment.
Reason for recall
GAGA Pro LLS systems was not in compliance with the FDA's Performance Standard for laser products.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1290-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.