{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "93136",
      "product_res_number": "Z-0099-2011",
      "event_date_initiated": "2006-06-08",
      "event_date_posted": "2010-10-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2010-11-03",
      "res_event_number": "56282",
      "product_code": "LNX",
      "product_description": "SoftWeb version 4.0.4.10.1.\nSCC Soft Computer, 5400 Tech Data Drive, Clearwater, FL 33760.\n\nManufacture Date: 05/16/2006.",
      "code_info": "version 4.0.4.10.1.",
      "firm_fei_number": "1000307651",
      "recalling_firm": "SCC Soft Computer",
      "address_1": "5400 Tech Data Drive",
      "city": "Clearwater",
      "state": "FL",
      "postal_code": "33760",
      "additional_info_contact": "727-789-0100",
      "reason_for_recall": "If a case number is re-used in SoftWeb with SoftPath, the SoftPath case is linked to the original MRN in SoftWeb. This causes SoftPath cases being linked to the wrong patient in SoftWeb.  Incorrect results on the patient with original MRN and no results on the patient with the second MRN (and the reused case number) are displayed in SoftWeb Results Query.  SCC Soft Computer issued a Correction for",
      "root_cause_description": "Software design",
      "action": "SCC Soft Computer issued a Risk-to-Health notification with Client Notification Verbiage to the affected client using SCC Soft Computer's proprietary Task Management System on June 8, 2006.  SCC recommended SoftPath/SoftWeb users NOT re-use SoftPath case numbers when cases are cancelled.  The generic option setting \"Specimen  Registration - Standard Settings - Minimum Time to Reactivate Case Number\" should be set to \"0\" so the user is not prompted to reuse the same case number.  Client was asked to acknowledge receipt of the task and grant permission to load the required software correction.",
      "product_quantity": "1",
      "distribution_pattern": "Nationwide Distribution: 1 hospital in Alaska.",
      "openfda": {
        "k_number": [
          "K921846"
        ]
      }
    }
  ]
}