{
  "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": "Waukesha",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81297",
      "recalling_firm": "GE Healthcare, LLC",
      "address_1": "3000 N Grandview Blvd",
      "address_2": "N/A",
      "postal_code": "53188-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "NY",
      "recall_number": "Z-0195-2019",
      "product_description": "Centricity Universal Viewer with Cross Enterprise Display This impacts product versions 6.0 SP1 and higher.",
      "product_quantity": "1",
      "reason_for_recall": "Remote comparison studies displayed may be associated with the wrong patient, without a caution icon present.",
      "recall_initiation_date": "20180830",
      "center_classification_date": "20181018",
      "termination_date": "20220831",
      "report_date": "20181024",
      "code_info": "SYSTEM ID: 315470CPUWPV   UDI #: 8406821038  00DE #: 2090255-001"
    }
  ]
}