{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "25329",
      "product_res_number": "Z-0438-03",
      "event_date_initiated": "2002-12-16",
      "event_date_posted": "2003-01-23",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-03-19",
      "res_event_number": "25169",
      "k_numbers": [
        "K013373",
        "K990092"
      ],
      "product_description": "PO2 electrode for Roche AVL OMNI Analyzers.  Catalog number BP1734.",
      "code_info": "All PO2 electrodes are affected.",
      "firm_fei_number": "1823260",
      "recalling_firm": "Roche Diagnostics Corp.",
      "address_1": "9115 Hague Road",
      "city": "Indianapolis",
      "state": "IN",
      "postal_code": "46250-0457",
      "additional_info_contact": "800-428-5074",
      "reason_for_recall": "Air bubbles trapped in the PO2 electrode will cause falsely elevated patient test results.",
      "root_cause_description": "Other",
      "action": "An urgent device correction letter dated 12/16/02 was sent to each customer.  The letter advised of the problem and instructed customers to follow a strict quality control regime to ensure proper electrode performance.  Customers were instructed how to automatically lock the affected parameter so that patient results will not be reported if QC performance violates the customer''s programmed rules.",
      "product_quantity": "695",
      "distribution_pattern": "United States",
      "openfda": {}
    }
  ]
}