{
  "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": "Greenville",
      "state": "SC",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68798",
      "recalling_firm": "AGFA Healthcare Corp.",
      "address_1": "10 S Academy St",
      "address_2": "N/A",
      "postal_code": "29601-2632",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Other",
      "distribution_pattern": "US in the state of WV",
      "recall_number": "Z-2176-2014",
      "product_description": "Agfa Digital Radiography X-Ray System DX-D 100    Product Usage:  Is indicated for use in providing diagnostic quality images to aid the physician with diagnoses.",
      "product_quantity": "1",
      "reason_for_recall": "Unit was mislabeled with a factory label showing 32 KW output power.",
      "recall_initiation_date": "20140513",
      "center_classification_date": "20140809",
      "termination_date": "20140813",
      "report_date": "20140820",
      "code_info": "Serial Number A5410000042"
    }
  ]
}