{
  "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": "76260",
      "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": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distribution was made to medical facilities in AZ, CA, CO, FL, HI, IL, MA, MD, MI, MO, NY, OH, PA, SC, TN, UT, and WI.  There was no foreign/government/military distribution.",
      "recall_number": "Z-1176-2017",
      "product_description": "Merge PACS software.  The firm name on the label is Merge Healthcare, Hartland, WI.",
      "product_quantity": "29 sites have the potentially affected software",
      "reason_for_recall": "Potential exists for an incorrect patient image being displayed which could result in the delay in diagnosis or treatment.",
      "recall_initiation_date": "20160404",
      "center_classification_date": "20170209",
      "termination_date": "20190408",
      "report_date": "20170215",
      "code_info": "Version 7.0.1"
    }
  ]
}