{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Guangzhou",
      "state": "N/A",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91969",
      "recalling_firm": "GAGA PRO LIGHTING EQUIPMENT CO.,",
      "address_1": "1238 Longjiao Road",
      "address_2": "Industrial Area",
      "postal_code": "N/A",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-1290-2023",
      "product_description": "GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Light Show (LLS)projectors for the purposes of demonstration and entertainment.",
      "product_quantity": "11 units",
      "reason_for_recall": "GAGA Pro LLS systems was not in compliance with the FDA's Performance Standard for laser products.",
      "recall_initiation_date": "20220923",
      "center_classification_date": "20230329",
      "report_date": "20230405",
      "code_info": "GA-RGB3000, GA-A4-W10000, GA-ML500-8, GA-RGB8000, GA-RGB4000, GA-RGB5000,  GA-G4000M, and GA-ML1800"
    }
  ]
}