{
  "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": "69508",
      "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 including the states of CO, NY, MO, LA, ME, CA, MI, AZ, CT and FL.",
      "recall_number": "Z-0223-2015",
      "product_description": "Nidek Excimer Laser Corneal Surgery System, model EC-5000 CXIII.  Opthalmic Device. The system is composed as a laser generator which produces an excimer laser radiation of wavelength 193nm, a beam delivery unit, an optical system for observation, a gas system and a computer for system control.",
      "product_quantity": "14 units",
      "reason_for_recall": "Contact failure in F1 and F4 fuse holders was detected on the EC-5000 CXIII Excimer Laser Corneal Surgery System that could cause a serious adverse event for the patient.",
      "recall_initiation_date": "20120806",
      "center_classification_date": "20141117",
      "termination_date": "20141117",
      "report_date": "20141126",
      "code_info": "Serial numbers:  530054  530055  530070  530073  530078  530082  530086  530087  530098  530106  530121  530123  530150  530155"
    }
  ]
}