{
  "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": "American Fork",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73977",
      "recalling_firm": "Novarad Corporation",
      "address_1": "752 E 1180 S Ste 200",
      "address_2": "N/A",
      "postal_code": "84003-3561",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide. 3 Canadian and 33 foreign consignees. No VA/gov/military.",
      "recall_number": "Z-1613-2016",
      "product_description": "NovaPACS \u0013 Diagnostic Viewer versions 8.3.7, 8.4.2, 8.4.3, and 8.4.4.  Novarad Corporation",
      "product_quantity": "2,386",
      "reason_for_recall": "The SUV values that are being calculated in the PET/CT fusion tool are incorrect.",
      "recall_initiation_date": "20151116",
      "center_classification_date": "20160506",
      "termination_date": "20160817",
      "report_date": "20160518",
      "code_info": "Versions 8.3.7, 8.4.2, 8.4.3, and 8.4.4"
    }
  ]
}