{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Charlotte",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71570",
      "recalling_firm": "McKesson Technologies, Inc.",
      "address_1": "10735 David Taylor Dr Ste 100",
      "address_2": "N/A",
      "postal_code": "28262-1288",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution including Puerto Rico and to the states of : CA, CO., CT, FL, GA, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NH, NJ, NM, NY, NC, OH, OK, OA, PA, SC, SD, TN, TX, VT, VA, WV and WY.",
      "recall_number": "Z-2263-2015",
      "product_description": "Paragon Laboratory Management",
      "product_quantity": "128",
      "reason_for_recall": "For Paragon Laboratory Management 12.1 and 12.1.1 releases, if used with Microsoft SQL Server 2012, the Final Cumulative Report may incorrectly display the data.",
      "recall_initiation_date": "20140615",
      "center_classification_date": "20150727",
      "termination_date": "20220201",
      "report_date": "20150805",
      "code_info": "Model 12.1 and 12.1.1"
    }
  ]
}