{
  "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": "70335",
      "recalling_firm": "Nidek Inc",
      "address_1": "47651 Westinghouse Dr",
      "address_2": "",
      "postal_code": "94539-7474",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Visit",
      "distribution_pattern": "Nationwide Distribution- including the states of CA, MI, NY, IL, NH, KS, NY, UT, IA, WI, TX, and FL.",
      "recall_number": "Z-1127-2015",
      "product_description": "MC-500 Multicolor Laser Photocoagulator;    Indicated for use in retinal photocoagulation for treatment of ocular fundus diseases like diabetic retinopathy, age-related macular degeneration, retinopathy of prematurity and retinal detachment.",
      "product_quantity": "16 units in commerce",
      "reason_for_recall": "The spot size control of the scan delivery unit of the MC-500 Multicolor Laser Photocoagulator may turn by itself.",
      "recall_initiation_date": "20120327",
      "center_classification_date": "20150219",
      "termination_date": "20150219",
      "report_date": "20150225",
      "code_info": "Serial numbers: 20023,20039, 20040, 20042, 20047, 20049, 20050, 20051, 20052, 20062, 20063, 20064, 20066, 20067, 20068, 20076",
      "more_code_info": ""
    }
  ]
}