{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Terminated",
      "city": "Issaquah",
      "state": "WA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85807",
      "recalling_firm": "Siemens Medical Solutions USA, Inc.",
      "address_1": "22010 SE 51st St",
      "address_2": "N/A",
      "postal_code": "98029-7298",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "U.S.: AZ, CA, FL, GA, IL, KY, MA, MI, MN, NJ, NY, OH, OK, OR, PA, TX, VA, WA and WV.    O.U.S; Canada",
      "recall_number": "Z-0090-2021",
      "product_description": "ACUSON AcuNav Volume Intracardiac Echocardiography Catheter 12.5F",
      "product_quantity": "N/A",
      "reason_for_recall": "Due to adverse events received by the firm for left atrial perforations and Atrioventricular Node block.",
      "recall_initiation_date": "20200522",
      "center_classification_date": "20201008",
      "termination_date": "20211015",
      "report_date": "20201014",
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