{
  "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": "26128",
      "product_res_number": "Z-0692-03",
      "event_date_initiated": "2003-01-30",
      "event_date_posted": "2003-03-29",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-06-01",
      "res_event_number": "25601",
      "k_numbers": [
        "K922823"
      ],
      "product_description": "Access 2 Immunoassay System",
      "code_info": "All fielded 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": "False results from secondary pour off tubes",
      "root_cause_description": "Other",
      "action": "Customers with the Access 2 instrument were informed of the recall issue by letter dated 1/30/2003. Those with the LXi 725 were informed by a letter dated 2/5/2003. The letters caution not to use certian Pour off tubes.",
      "product_quantity": "718",
      "distribution_pattern": "Nationwide and Canada",
      "openfda": {}
    }
  ]
}