{
  "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": "85513",
      "recalling_firm": "Philips North  America, LLC",
      "address_1": "3000 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "Worldwide distribution including one unit distributed to Iowa.",
      "recall_number": "Z-1922-2020",
      "product_description": "Philips Brilliance iCT SP Computed Tomography X-Ray System; Model # 728311",
      "product_quantity": "2",
      "reason_for_recall": "The bolt affixing the cooling unit to the rotor was not tightened to specification on the Philips Brilliance iCT systems.",
      "recall_initiation_date": "20200406",
      "center_classification_date": "20200506",
      "termination_date": "20220916",
      "report_date": "20200513",
      "code_info": "Serial # 200044    Additional unit as off 5/22/20:  200026",
      "more_code_info": ""
    }
  ]
}