{
  "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": "2026-04-08",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87826",
      "recalling_firm": "Abbott Laboratories Inc. (St Jude Medical)",
      "address_1": "1 Saint Jude Medical Dr",
      "address_2": "",
      "postal_code": "55117-1789",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US and AUSTRALIA, EGYPT, SOUTH AFRICA, BELGIUM, COLOMBIA, UNITED KINGDOM, COSTA RICA, ISRAEL, SOUTH KOREA, SINGAPORE, TAIWAN",
      "recall_number": "Z-1549-2021",
      "product_description": "NeuroTherm NT2000iX Radiofrequency (RF) Generator, Model Number RFG-NT-2000",
      "product_quantity": "318 units",
      "reason_for_recall": "Potential capacitor failure which typically manifests as in inability to provide output on one or more channels.  In some instances, users reported a charring/smoky odor or emission.",
      "recall_initiation_date": "20210422",
      "center_classification_date": "20210510",
      "termination_date": "20230202",
      "report_date": "20210519",
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      "more_code_info": ""
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