{
  "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": [
    {
      "country": "United States",
      "city": "Billerica",
      "address_1": "829 Middlesex Tpke",
      "reason_for_recall": "During factory testing, we discovered that Gemini systems could, in rare circumstances, experience a fault that leads to a state in which X-rays are being produced but the X-ray indicator lights (located on the operator's console and on both ends of the tunnel) are not illuminated.",
      "address_2": "",
      "product_quantity": "125 systems",
      "code_info": "Gemini systems",
      "center_classification_date": "20150814",
      "distribution_pattern": "Worldwide Distribution - US Distribution to the states of : NY, FL, TN, PA, NJ, DE, ME, TX, CT, MS, NC, MD, MO, VA, DC, NV and GA., and to the countries of : Saudi Arabia, Indonesia, Canada, Netherlands, Hong Kong, Lebanon and Kazakhstan.",
      "state": "MA",
      "product_description": "American Science & Engineering Inc,Gemini Cabinet X-ray system.",
      "report_date": "20150826",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "American Science & Engineering, Inc.",
      "recall_number": "Z-2206-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71696",
      "termination_date": "20170222",
      "more_code_info": "",
      "recall_initiation_date": "20150522",
      "postal_code": "01821-3907",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}