{
  "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": "71838",
      "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": "US Nationwide  Distribution to the states of : Arizona, Minnesota, State of Washington, Wyoming and Ohio.   Internationally to Canada.",
      "recall_number": "Z-2383-2015",
      "product_description": "Philips DigitalDiagnost Release 4.0.3, Release 4.1/4.1.1. excluding systems with SP1      Product Usage:  The DigitalDiagnost is intended for use in generating radiographic images of human anatomy by qualified/trained doctors or technicians.",
      "product_quantity": "62",
      "reason_for_recall": "The system is designed to emit a beep upon termination of an exposure. However, if the system has been powered on for over 12 hours, the system will no longer emit this signal due to a defect in the Microsoft Windows 7 operating system.",
      "recall_initiation_date": "20150323",
      "center_classification_date": "20150822",
      "termination_date": "20170117",
      "report_date": "20150902",
      "code_info": "DigitalDiagnost"
    }
  ]
}