{
  "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": [
    {
      "country": "United States",
      "city": "Hartland",
      "address_1": "900 Walnut Ridge Dr",
      "reason_for_recall": "The International Normalized Ratio (INR) value displayed in the study report does not match the value that is imported on the pre-procedure labs screen from HL7",
      "address_2": "",
      "product_quantity": "37",
      "code_info": "Software versions 8.10, 9.10, 9.20.",
      "center_classification_date": "20160804",
      "distribution_pattern": "The medical facilities who currently have the affected versions are located nationwide.  There was government distribution but no military or foreign distribution.",
      "state": "WI",
      "product_description": "Merge HEMO software.",
      "report_date": "20160810",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Merge Healthcare, Inc.",
      "recall_number": "Z-2341-2016",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "74577",
      "termination_date": "20170626",
      "more_code_info": "",
      "recall_initiation_date": "20120702",
      "postal_code": "53029-8347",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}