{
  "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": "2026-08-12",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Hartland",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99391",
      "recalling_firm": "Merge Healthcare, Inc.",
      "address_1": "900 Walnut Ridge Dr",
      "address_2": "",
      "postal_code": "53029-8347",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada, and UK.",
      "recall_number": "Z-2875-2026",
      "product_description": "Merge OrthoPACS, medical imaging diagnostic workstation",
      "product_quantity": "5 units",
      "reason_for_recall": "Thumbnails from a previously opened patient study may be displayed in the Thumbnail Bar while a different patient study is currently open.",
      "recall_initiation_date": "20260630",
      "center_classification_date": "20260804",
      "report_date": "20260812",
      "code_info": "UDI/DI (01)00842000101154(10)9.4.0.P02(11)260302, with Affected Versions:  9.4, 9.4 P01, and 9.4 P02.",
      "more_code_info": ""
    }
  ]
}