{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Hartland",
      "address_1": "900 Walnut Ridge Dr",
      "reason_for_recall": "Studies coming over via telmed were missing patient's DOB, procedure, and referring physician.",
      "address_2": "",
      "product_quantity": "109 sites have the affected versions",
      "code_info": "Versions: V6.0 MR4 CU 1-11, 6.1.0, 6.1.1, 6.1.1.1, 6.1.2, 6.1.3, 6.1.3.1, 6.2.0, 6.2.1, 6.2.2, 6.2.2.1, and 6.2.3.",
      "center_classification_date": "20160729",
      "distribution_pattern": "Worldwide Distribution --  USA, New Zealand, and United Kingdom.",
      "state": "WI",
      "product_description": "Merge PACS software.  The firm name on the label is Merge Healthcare, Hartland, WI.     Intended to create and display two-dimensional and three-dimensional images of anatomy from a series of digitally acquired images.",
      "report_date": "20160810",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Merge Healthcare, Inc.",
      "recall_number": "Z-2301-2016",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "74648",
      "termination_date": "20190408",
      "more_code_info": "",
      "recall_initiation_date": "20160130",
      "postal_code": "53029-8347",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}