{
  "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": "2026-04-01",
    "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": "86205",
      "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": "Letter",
      "distribution_pattern": "Domestic Distribution:  IL, MO, NY, ND, MI, TX, FL, OH, UT, NE, MS, MN, DE, AR, CA, WI, MD, NC, NH, GA, VA, SC, PE, CT, NM, IN.    International Distribution: CA, BE, UK.",
      "recall_number": "Z-2944-2020",
      "product_description": "Merge PACS",
      "product_quantity": "125 total units",
      "reason_for_recall": "Measurements done on the Merge PACS generated MPR s may have incorrect measurements.",
      "recall_initiation_date": "20200806",
      "center_classification_date": "20200909",
      "termination_date": "20221130",
      "report_date": "20200916",
      "code_info": "Unique Device Identifier (UDI):  v8.1:   PACS:(01)00842000100805(10)8.1(11)191022 OrthoPACS: (01)00842000100805(10)8.1(11)191022  v81.1:   PACS: (01)00842000100805(10)8.1.1(11)200528 OrthoPACS: (01)00842000100805(10)8.1.1(11)200528   V8.1.2   PACS: (01)00842000100805(10)8.1.2(11)200709",
      "more_code_info": ""
    }
  ]
}