{
  "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": "2026-04-15",
    "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": "73316",
      "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 Nationwide Distribution",
      "recall_number": "Z-1245-2016",
      "product_description": "RT-5100 (Epic 5100) Refractor and RT 3100 Refractor:    Product Usage:  Instrument providing means of positioning spherical and cylindrical lenses, prisms and other optical devices in front of a subject\u0019s eye for purpose of determining refractive error and binocular functions.",
      "product_quantity": "2703 separate serial numbers",
      "reason_for_recall": "There has been a reoccurrence of an issue on the RT 5100 and RT 3100 Refractor of the Near Point Chart Arm lowering spontaneously with potential for slight injury to face or nose of patient.",
      "recall_initiation_date": "20160229",
      "center_classification_date": "20160324",
      "termination_date": "20180924",
      "report_date": "20160330",
      "code_info": "serial numbers: See attached distribution list.  128 RT -3100 and 2565 RT-5100."
    }
  ]
}