{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Glendale",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83438",
      "recalling_firm": "Gk Photonics Inc",
      "address_1": "717 Ridge Dr",
      "address_2": "N/A",
      "postal_code": "91206-1752",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Unknown",
      "recall_number": "Z-2092-2019",
      "product_description": "ClubMax Laser Projection Series",
      "product_quantity": "1291 total",
      "reason_for_recall": "The User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser projectors and could unintentionally expose the user and/or observers to high power laser radiation. It needs to be replaced for safety reasons.",
      "recall_initiation_date": "20190710",
      "center_classification_date": "20190807",
      "report_date": "20190814",
      "code_info": "ClubMax Laser Projection Series"
    }
  ]
}