{
  "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": "Studies that have QC, PDE, or HL7 ADT updates applied may fail to propagate via telmed protocol to the destination server and may fail to import on the destination server.",
      "address_2": "",
      "product_quantity": "160 sites potentially have the affected versions",
      "code_info": "Versions 6.6, 6.6.1, 6.6.2, 6.6.2.1, and 6.6.2.2",
      "center_classification_date": "20170616",
      "distribution_pattern": "USA (nationwide) Distribution was made to medical facilities.  There was no foreign/government/military distribution.",
      "state": "WI",
      "product_description": "Merge OrthoPACS software.  The firm name on the label is Merge Healthcare, Hartland, WI.",
      "report_date": "20170628",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Merge Healthcare, Inc.",
      "recall_number": "Z-2601-2017",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "77271",
      "termination_date": "20191015",
      "more_code_info": "",
      "recall_initiation_date": "20170524",
      "postal_code": "53029-8347",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}