{
  "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,
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  },
  "results": [
    {
      "cfres_id": "25915",
      "product_res_number": "Z-0570-03",
      "event_date_initiated": "2003-01-20",
      "event_date_posted": "2003-02-25",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-07-26",
      "res_event_number": "25485",
      "k_numbers": [
        "K003677"
      ],
      "product_description": "AcT 5 diff Cap Pierce Hematology Analyzer\n\n864.5220 Automated differential cell counter",
      "code_info": "Not applicaable.",
      "firm_fei_number": "2050012",
      "recalling_firm": "Beckman Coulter Inc",
      "address_1": "200 South Kraemer Blvd W 337",
      "city": "Brea",
      "state": "CA",
      "postal_code": "92822",
      "additional_info_contact": "Lynne McBride\n714-961-3626",
      "reason_for_recall": "Failure to cycle properly ammong samples.",
      "root_cause_description": "Other",
      "action": "Customers were sent a letter dated January 20, 2003 that describes this situation and provides modified operating instructions to prevent the occurence.",
      "product_quantity": "351",
      "distribution_pattern": "US and Canada",
      "openfda": {}
    }
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}