{
  "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": "Buffalo Grove",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74106",
      "recalling_firm": "Sedecal USA, Inc.",
      "address_1": "230 Lexington Dr",
      "address_2": "N/A",
      "postal_code": "60089-6930",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution - TX, OH, NY, MD, IN, PA, DE, WA, NH, AZ, GA, NC, UT, VT, CA, LA, NJ, MN, FL, WI, HI, IA, MA, ME, TN, CT, ID, MI, AR and KS.",
      "recall_number": "Z-1691-2016",
      "product_description": "Sedecal SA Mobile Diagnost w DR x-ray system",
      "product_quantity": "US - 145",
      "reason_for_recall": "Due to a software defect, the system may sporadically apply the default x ray exposure parameters for an adult ( patient type : Normal ) even though the patient type \" Newborn\" was selected and is displayed in the generator control area of the Eleva User Interface.",
      "recall_initiation_date": "20150323",
      "center_classification_date": "20160603",
      "termination_date": "20180309",
      "report_date": "20160615",
      "code_info": "System Code 712001"
    }
  ]
}