{
  "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": "69531",
      "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": "Visit",
      "distribution_pattern": "US Distribution in the states of: CA, NE, and NY.",
      "recall_number": "Z-0222-2015",
      "product_description": "MC-500 Multicolor Laser Photocoagulator using software version 2.20.  Opthalmic device used for retinal photocoagulation for treatment of ocular fundus diseases.",
      "product_quantity": "5",
      "reason_for_recall": "Retrospective review found that a Engineering Change Order initiated in May 2013 for a memory function problem was not reported as required.",
      "recall_initiation_date": "20130524",
      "center_classification_date": "20141117",
      "termination_date": "20141117",
      "report_date": "20141126",
      "code_info": "MC-500; Serial numbers: 50011,  50382, 50425, 50558, 50609"
    }
  ]
}