{
  "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": [
    {
      "country": "United States",
      "city": "Greenville",
      "address_1": "10 S Academy St",
      "reason_for_recall": "Patient name displayed (printed) on the Patient Report was the  wrong patient name.",
      "address_2": "",
      "product_quantity": "14",
      "code_info": "Software IMPAX RIS 58 and higher",
      "center_classification_date": "20140203",
      "distribution_pattern": "CA, FL, GA, ME, OH, OR, SC, SD, TX and Canada",
      "state": "SC",
      "product_description": "IMPAX RIS QDOC 5.8",
      "report_date": "20140212",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "AGFA Corp.",
      "recall_number": "Z-0919-2014",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "67275",
      "termination_date": "20140228",
      "more_code_info": "",
      "recall_initiation_date": "20140108",
      "postal_code": "29601-2632",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}