{
  "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": [
    {
      "status": "Terminated",
      "city": "Wayne",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77712",
      "recalling_firm": "Konica Minolta, Inc.",
      "address_1": "411 Newark Pompton Tpke",
      "address_2": "N/A",
      "postal_code": "07470-6657",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "CA, CO, KY, FL, NJ, NY, IA TX, & WA",
      "recall_number": "Z-2769-2017",
      "product_description": "Diagnostics Ultrasound System  Ultrasounds System Sonimage HS1",
      "product_quantity": "36 units",
      "reason_for_recall": "The Doppler velocity measurement on the Sonimage HS1 ultrasound system is not accurate.",
      "recall_initiation_date": "20170424",
      "center_classification_date": "20170726",
      "termination_date": "20180124",
      "report_date": "20170802",
      "code_info": "UDI   04560141940031  04560141944534  04560141945463  04560141946385      V1.31R02  V1.31R04  V1.31R05  V1.31R06 (V131R02 SW and later version)"
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}