{
  "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": "Waukesha",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70701",
      "recalling_firm": "GE Healthcare",
      "address_1": "3000 N Grandview Blvd",
      "address_2": "N/A",
      "postal_code": "53188-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the state of CA., and Internationally to Italy and Japan.",
      "recall_number": "Z-1395-2015",
      "product_description": "GE Discovery MR950 MRI  system",
      "product_quantity": "5 units (2 in US)",
      "reason_for_recall": "The alignment lasers are missing the labels required by radiation safety regulations.",
      "recall_initiation_date": "20141024",
      "center_classification_date": "20150501",
      "termination_date": "20150506",
      "report_date": "20150513",
      "code_info": "Model Number -  Discovery MR950"
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}