{
  "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": "A migrated study that has annotations will display the annotations, but when a prior study is loaded that should have annotations, the second study will not display annotations.",
      "address_2": "",
      "product_quantity": "98 sites potentially have the affected versions",
      "code_info": "Versions 6.6, 6.6.1, and 6.6.2",
      "center_classification_date": "20170622",
      "distribution_pattern": "Distribution was made nationwide to medical facilities.  There was no foreign/government/military distribution.",
      "state": "WI",
      "product_description": "Merge OrthoPACS software.",
      "report_date": "20170628",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Merge Healthcare, Inc.",
      "recall_number": "Z-2620-2017",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "77265",
      "termination_date": "20190628",
      "more_code_info": "",
      "recall_initiation_date": "20170524",
      "postal_code": "53029-8347",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}