{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "31730",
      "product_res_number": "Z-0635-04",
      "event_date_initiated": "2004-02-13",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-05-08",
      "res_event_number": "28379",
      "product_code": "GKL",
      "product_description": "CXP software, Part No. 623560, version 1.0",
      "code_info": "Version 1.0",
      "firm_fei_number": "2050012",
      "recalling_firm": "Beckman Coulter Inc",
      "address_1": "200 S Kraemer Blvd",
      "city": "Brea",
      "state": "CA",
      "postal_code": "92821-6208",
      "additional_info_contact": "Kathleen Jaker\n714-961-3666",
      "reason_for_recall": "Software anomaly. Sample ID and the Run Date may become fixed within a header on the FlowPAGE printout. All samples subsequently run, with results printed using the FlowPAGE print format, will have the fixed Sample ID and Run Date, rather than the correct Sample ID and Run Date.",
      "root_cause_description": "Other",
      "action": "Firm sent modified operating instructions to users on 13 February 2004.",
      "product_quantity": "21",
      "distribution_pattern": "Nationwide and Canada",
      "openfda": {
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        "device_name": "Counter, Cell, Automated (Particle Counter)",
        "medical_specialty_description": "Hematology",
        "regulation_number": "864.5200",
        "device_class": "2",
        "registration_number": [
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