{
  "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": "Twinsburg",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79160",
      "recalling_firm": "Hitachi Medical Systems America Inc",
      "address_1": "1959 Summit Commerce Park",
      "address_2": "N/A",
      "postal_code": "44087-2371",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed in 21 states: AR, AZ, CA, CO, FL, GA, IA, IL, IN, MA, MO, NC, NY, OK, OR, PA, SC, TX, VA, WA, WV.",
      "recall_number": "Z-0816-2018",
      "product_description": "Ultrasound Transducer, Model Number: UST-5550-R, is used in conjunction with a diagnostic ultrasound system evaluation during robotic and non-robotic intra-operative and laparoscopic procedures.",
      "product_quantity": "55",
      "reason_for_recall": "The ultrasound probe may not have adequate protection against electrical shock hazards.",
      "recall_initiation_date": "20171020",
      "center_classification_date": "20180301",
      "termination_date": "20200416",
      "report_date": "20180307",
      "code_info": "17  21  32  37  38  39  41  43  45  46  48  57  58  59  61  63  64  69  73  77  78  81  82  86  87  92  96  97  99  107  108  109  114  115  116  118  120  121  122  126  129  130  132  135  139  140  141  143  144  147  148  151  155"
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}