{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Sesto Fiorentino",
      "state": "N/A",
      "country": "Italy",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79547",
      "recalling_firm": "ESAOTE S.P.A.",
      "address_1": "Sesto Fiorentino",
      "address_2": "Via Degli Olmi 11",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US distribution in the states: AZ, FL, OK, PA, and TX.",
      "recall_number": "Z-1137-2018",
      "product_description": "MyLab Ultrasound System; Models 6100, 6150, 6200, 6250; PA023E Probe 7.5/10",
      "product_quantity": "1",
      "reason_for_recall": "The ultrasound system used in certain settings may result in overheating of the ultrasound probe head.",
      "recall_initiation_date": "20180103",
      "center_classification_date": "20180320",
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      "report_date": "20180328",
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