{
  "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": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71764",
      "recalling_firm": "Philips Electronics North  America Corporation",
      "address_1": "3000 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of NY, WI, MA, AL, FL, GA, RI, CA, KS, and  TX, and the countries of Canada, Australia, Austria, Belgium, France, Germany, Ireland, Italy, Netherlands, New Zealand, Portugal, South Africa, Spain, and Switzerland.",
      "recall_number": "Z-0766-2016",
      "product_description": "Philips Healthcare TraumaDiagnost; Codes: 72001, 720011, 720013, 720020; A radiological examination unit for emergency work and routine skeletal diagnosis.",
      "product_quantity": "399 distributed, 262 are subject to this event",
      "reason_for_recall": "If arm is not fastened securely it could fall down.",
      "recall_initiation_date": "20150722",
      "center_classification_date": "20160205",
      "termination_date": "20201014",
      "report_date": "20160217",
      "code_info": "All TraumaDiagnost products that were delivered before the week of July 2, 2007.",
      "more_code_info": ""
    }
  ]
}