{
  "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": "Mountain View",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79568",
      "recalling_firm": "Siemens Medical Solutions USA, Inc.",
      "address_1": "685 E Middlefield Rd",
      "address_2": "N/A",
      "postal_code": "94043-4045",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was made to medical facilities in AZ, CA, CT, FL, IL, IN, KS, KY, MI, MN, MO, NJ, NY, NC, OH, PA, TX, VA, and WA.  There was no military/government distribution.    Foreign distribution was made to Argentina, Australia, Austria, Belgium, Bosnia Herzeg, Colombia, Croatia, Denmark, France, Germany, India, Ireland, Israel, Italy, Japan, Mexico, New Zealand, Philippines, Poland, Republic Korea, Romania, Singapore, Slovakia, Spain, Sweden, Taiwan, Thailand, Turkey, UAE, and Vietnam.",
      "recall_number": "Z-1200-2018",
      "product_description": "ACUSON SC2000 Ultrasound System.  The firm name on the label is Siemens Medical Solutions USA, Inc., Buffalo Grove, IL.",
      "product_quantity": "229 systems",
      "reason_for_recall": "The ECG signal may flatline due to electromagnetic interference during the use of electrosurgical equipment.",
      "recall_initiation_date": "20180305",
      "center_classification_date": "20180507",
      "termination_date": "20210226",
      "report_date": "20180516",
      "code_info": "Software versions VB20A, VB20B, or VB20C that have a common physio module (CPM) (known by customers as the ECG (physio) hardware) installed at revision 4"
    }
  ]
}