{
  "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": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86416",
      "recalling_firm": "Philips North  America, LLC",
      "address_1": "3000 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1032",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "United States",
      "recall_number": "Z-3023-2020",
      "product_description": "ProxiDiagnost N90",
      "product_quantity": "71",
      "reason_for_recall": "Unexpected increase in peak tube potential (kV) will lead to an increased patient radiation dose.",
      "recall_initiation_date": "20191120",
      "center_classification_date": "20200930",
      "termination_date": "20240404",
      "report_date": "20201007",
      "code_info": "All ProxiDiagnost N90 systems are affected."
    }
  ]
}