{
  "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": "76859",
      "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": "Nationwide Distribution including AZ, CA, CO, FL, GA, KS, LA, MI, MO, OH, OK, TN, TX, VA, WA, WI, and WV.",
      "recall_number": "Z-1778-2017",
      "product_description": "Merge Hemo software.  The firm name on the labeling is Merge Healthcare, Hartland, WI.  Merge Hemo monitors, measures, and records physiologic data from a human patient undergoing a cardiac catheterization procedure",
      "product_quantity": "24 sites potentially have the affected versions",
      "reason_for_recall": "Use of the software may show an incorrect value to the user when viewing the Fractional Flow Reserve (FFR) results during recording.",
      "recall_initiation_date": "20160404",
      "center_classification_date": "20170411",
      "termination_date": "20190221",
      "report_date": "20170419",
      "code_info": "Versions 9.10.0, 9.20.0, 9.20.1, 9.20.2, 9.30.3,  and 9.40.0.",
      "more_code_info": ""
    }
  ]
}