{
  "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": [
    {
      "status": "Terminated",
      "city": "Clearwater",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77669",
      "recalling_firm": "Soft Computer Consultants, Inc.",
      "address_1": "5400 Tech Data Dr",
      "address_2": "N/A",
      "postal_code": "33760-3116",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to states of: CA, IL, LA, MA, MD, MI, MN, NJ, NY, PA, and TX.",
      "recall_number": "Z-2865-2017",
      "product_description": "SoftLab Software    Laboratory information system to be used in a medical research or clinical laboratory by knowledgeable, trained,",
      "product_quantity": "18 units",
      "reason_for_recall": "Display of lab results based on incorrect LOINC code/test descriptions for tests that were performed at a reference lab, saved incorrectly, and sent to systems that display the EMR.",
      "recall_initiation_date": "20170531",
      "center_classification_date": "20170802",
      "termination_date": "20200804",
      "report_date": "20170809",
      "code_info": "Versions 4.5.4.3, 4.5.4.5, 4.5.4.6, 4.5.4.8, 4.5.4.9, 4.5.4.20, 4.5.4.30, 4.5.4.40, 4.5.5.0, 4.5.5.10, and 4.5.5.20"
    }
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}