{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Chatsworth",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74838",
      "recalling_firm": "Northridge Tri-Modality Imaging,",
      "address_1": "9457 de Soto Ave",
      "address_2": "N/A",
      "postal_code": "91311-4920",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "USA  Distribution",
      "recall_number": "Z-2833-2016",
      "product_description": "TriFoillmaging Triumph/Triumph II Research CT scanners.",
      "product_quantity": "3",
      "reason_for_recall": "The Firm has determined that several Triumph/Triumph II Research CT scanners produced by Northridge Trimodality Imaging, inc dba TriFoillmaging (or by Gamma Medica-Ideas, Inc and field upgraded with a replacement  x-ray tube) may be out of compliance with 21 CFR 1020.40 (Cabinet X-ray standards)",
      "recall_initiation_date": "20160524",
      "center_classification_date": "20160930",
      "termination_date": "20161006",
      "report_date": "20161012",
      "code_info": "n/a"
    }
  ]
}