{
  "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": "Hartland",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75419",
      "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": "Distribution was made nationwide and to the Virgin Islands.  Foreign distribution was made to the Bahamas.",
      "recall_number": "Z-0399-2017",
      "product_description": "Merge LIS software.",
      "product_quantity": "413 sites potentially have the affected software",
      "reason_for_recall": "There is a potential for duplicate container numbers to be created for patients.",
      "recall_initiation_date": "20150305",
      "center_classification_date": "20161111",
      "termination_date": "20190412",
      "report_date": "20161123",
      "code_info": "Versions: 4.0.1 and earlier."
    }
  ]
}