{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Hartland",
      "address_1": "900 Walnut Ridge Dr",
      "reason_for_recall": "When measuring a lesion on an unmagnified mammography image then performing the same measurement on an image magnified by the Hologic imager (different image), the measurements are not the same.",
      "address_2": "",
      "product_quantity": "49 sites potentially have the affected versions",
      "code_info": "Software versions 6.0.2.0 MR2, 6.0.3.0 MR3, 6.0.3.1 MR3 CU1",
      "center_classification_date": "20160808",
      "distribution_pattern": "Worldwide Distribution --  USA and Australia.",
      "state": "WI",
      "product_description": "Merge PACS software.  The firm name on the label is Merge Healthcare, Inc., Hartland, WI.    Intended to create and display two-dimensional and three-dimensional images of anatomy from a series of digitally acquired images.",
      "report_date": "20160817",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Merge Healthcare, Inc.",
      "recall_number": "Z-2363-2016",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "74776",
      "termination_date": "20161025",
      "more_code_info": "",
      "recall_initiation_date": "20160205",
      "postal_code": "53029-8347",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}