{
  "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": [
    {
      "country": "United States",
      "city": "Danvers",
      "address_1": "14 Electronics Ave",
      "reason_for_recall": "While transporting the portable machine with the retrofit equipment in a backwards motion, there is potential for foot injury from the underside of the detector bin of the retrofit unit.",
      "address_2": "",
      "product_quantity": "16 units",
      "code_info": "Model Number GMR40.  Serial numbers 00001 through 00016.",
      "center_classification_date": "20180417",
      "distribution_pattern": "US Distribution . Only one consignee was shipped 16 units of the affected device.",
      "state": "MA",
      "product_description": "Solid state x-ray imager (flat panel/digital imager)      Solid state x-ray imager (flat panel/digital imager)  Medical",
      "report_date": "20180425",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "NeuroLogica Corporation",
      "recall_number": "Z-1391-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "79628",
      "termination_date": "20180814",
      "more_code_info": "",
      "recall_initiation_date": "20180112",
      "postal_code": "01923-1011",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}