{
  "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": "Barrington",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64545",
      "recalling_firm": "Ge Medical Systems Information T",
      "address_1": "540 W Northwest Hwy",
      "address_2": "N/A",
      "postal_code": "60010-3051",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide, Worldwide",
      "recall_number": "Z-1782-2017",
      "product_description": "Centricity PACS Web Diagnostic (WebDX) by GE Healthcare Dynamic Imaging Solutions is a device that receives medical images (including mammograms) and data from various imaging sources within the system or across computer networks at distributed locations.",
      "product_quantity": "118",
      "reason_for_recall": "It was reported from a complaint that study category labels of \"Prior\" and \"Baseline\" and hanging position appeared incorrectly swapped when the hanging protocol for three comparison studies is manually applied from the patient folder.",
      "recall_initiation_date": "20130218",
      "center_classification_date": "20170411",
      "termination_date": "20170731",
      "report_date": "20170419",
      "code_info": "Versions 1.0, 1.1, 2.0, 2.1",
      "more_code_info": ""
    }
  ]
}