{
  "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": "25914",
      "product_res_number": "Z-0571-03",
      "event_date_initiated": "2002-12-10",
      "event_date_posted": "2003-02-25",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-04-21",
      "res_event_number": "25484",
      "k_numbers": [
        "K011342",
        "K962988"
      ],
      "product_description": "Coulter LH 700 Series and GEN S Hematology Analyzers\n\n864.5220 Automated differential cell counter",
      "code_info": "In the LH 700 series, all serial numbers up to AE1088.  In the GENS series, all instruments.",
      "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": "Device design allows for cross contamination issue to occur, possibly affecting assays and results reports.",
      "root_cause_description": "Other",
      "action": "Firm will check and shorten sweepflow tubing on a next visit basis during routine service visits.",
      "product_quantity": "447",
      "distribution_pattern": "Nationwide and Canada",
      "openfda": {}
    }
  ]
}