{
  "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": [
    {
      "country": "United States",
      "city": "Hartland",
      "address_1": "900 Walnut Ridge Dr",
      "reason_for_recall": "The patient name in the Halo title bar and the thumbnails do not match the name on displayed images.",
      "address_2": "",
      "product_quantity": "93 sites have the affected version",
      "code_info": "Versions: V6.0.2.0 MR2 and earlier",
      "center_classification_date": "20160810",
      "distribution_pattern": "The software was distributed to medical facilities nationwide.  Government distribution was made to MN.  Foreign distribution was made to Australia and to the United Kingdom.  There was no military distribution.",
      "state": "WI",
      "product_description": "Merge PACS software.  Product was distributed under the AMICAS label, Brighton, MA, but labeling was later changed to Merge Healthcare, Hartland, WI.",
      "report_date": "20160817",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Merge Healthcare, Inc.",
      "recall_number": "Z-2379-2016",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "74773",
      "termination_date": "20201005",
      "more_code_info": "",
      "recall_initiation_date": "20160130",
      "postal_code": "53029-8347",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}