{
  "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": [
    {
      "country": "United States",
      "city": "Andover",
      "address_1": "3000 Minuteman Rd",
      "reason_for_recall": "During recent evaluations of the Philips DigitalDiagnost C50 system, Philips identified a missing label.  This notification is intended to provide you with information regarding what the issue is, and relevant affected product, the actions you are required to take and the actions planned by Philips to correct the issue.  If you need any or further information or support concerning this issue, please contact your local Philips representative or Philips Customer Service: 1-800-722-9377.",
      "address_2": "",
      "product_quantity": "2",
      "code_info": "Product Number 712201    System Serial Number:    SN170053  SN180074",
      "center_classification_date": "20190920",
      "distribution_pattern": "Puerto Rico",
      "state": "MA",
      "product_description": "DigitalDiagnost C50, Stationary X-ray System",
      "report_date": "20191002",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Healthcare",
      "recall_number": "Z-2498-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83654",
      "termination_date": "20201027",
      "more_code_info": "",
      "recall_initiation_date": "20181221",
      "postal_code": "01810-1032",
      "voluntary_mandated": "FDA Mandated",
      "status": "Terminated"
    }
  ]
}