{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Fremont",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71527",
      "recalling_firm": "Nidek Inc",
      "address_1": "47651 Westinghouse Dr",
      "address_2": "N/A",
      "postal_code": "94539-7474",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of : CA, IL, MN, MO, OR, IL, UT RI, MA, WA, NE, NY, NJ, TX and WI.",
      "recall_number": "Z-2067-2015",
      "product_description": "Dual Delivery 4DD-1 of GYC-1000 Green Laser Photocoagulator system  GYC4DD-1:    The Nidek Green Laser Photocoagulator Model GYC- 1000 is indicated for use in ophthalmic surgical procedures, including retinal and macular photocoagulation, iridotomy and trabeculoplasty.",
      "product_quantity": "22 units",
      "reason_for_recall": "Accessories to the GYC-1000 laser were missing Laser Aperture labels.",
      "recall_initiation_date": "20150325",
      "center_classification_date": "20150714",
      "termination_date": "20150714",
      "report_date": "20150722",
      "code_info": "Model GYC4DD-1",
      "more_code_info": ""
    }
  ]
}