{
  "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": "Hartland",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76258",
      "recalling_firm": "Merge Healthcare, Inc.",
      "address_1": "900 Walnut Ridge Dr",
      "address_2": "N/A",
      "postal_code": "53029-8347",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Other",
      "distribution_pattern": "US Distribution was made to medical facilities in AL, IN, MI, PA and WI.",
      "recall_number": "Z-1180-2017",
      "product_description": "Merge RadSuite software.  The firm name on the label is Merge Healthcare, Hartland, WI.",
      "product_quantity": "8 sites have the potentially affected version",
      "reason_for_recall": "The values provided from the Pixel Value tool do not appear to be correct, which may result in potential patient injury or delay in diagnosis or treatment.",
      "recall_initiation_date": "20151117",
      "center_classification_date": "20170209",
      "termination_date": "20170210",
      "report_date": "20170215",
      "code_info": "Version V8.30.7.8"
    }
  ]
}