{
  "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": "2026-04-29",
    "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": "68485",
      "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 only.",
      "recall_number": "Z-1853-2014",
      "product_description": "RT-5100 Refractor and RT-3100 Refractor;    Distributed by MARCO Opthalmic:  Manufactured by NIDEK CO., Ltd., Aichi, Japan.    Instrument provides means of positioning spherical and cylindrical lenses, prisms and other optical devices in front of a subject's eyes for purpose of determining refractive error and binocular functions.",
      "product_quantity": "~4,285 units RT-5100; 167 units of RT-3100",
      "reason_for_recall": "Near Point Chart Arm of RT 5100 and RT-3100 Refractors may lower spontaneously with potential for patient injury.",
      "recall_initiation_date": "20140609",
      "center_classification_date": "20140623",
      "termination_date": "20151030",
      "report_date": "20140702",
      "code_info": "RT-5100 and RT-3100, various serial numbers."
    }
  ]
}