{
  "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": [
    {
      "status": "Terminated",
      "city": "Hartland",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76541",
      "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": "E-Mail",
      "distribution_pattern": "US Distribution was made to medical facilities in CA, MT, PA, and TX.   There was no foreign/military/government distribution.",
      "recall_number": "Z-1426-2017",
      "product_description": "DR Systems Unity PACS software, now known as Merge Unity PACS",
      "product_quantity": "9 sites potentially have the affected version",
      "reason_for_recall": "Reports were missing demographic header information when they were faxed to referring physicians.",
      "recall_initiation_date": "20160408",
      "center_classification_date": "20170309",
      "termination_date": "20170317",
      "report_date": "20170315",
      "code_info": "Version 11.0"
    }
  ]
}