{
  "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": "27322",
      "product_res_number": "Z-0012-04",
      "event_date_initiated": "2003-05-08",
      "event_date_posted": "2003-10-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-12-09",
      "res_event_number": "26231",
      "k_numbers": [
        "K953239"
      ],
      "product_description": "Roche/Hitachi Modular Analytics P clinical chemistry analyzer; Modular P.  Catalog number 766-8156.",
      "code_info": "All units with current software versions (v 06-06 and 07-01).",
      "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": "800-428-2336",
      "reason_for_recall": "Incorrect results, without a data flag, reported if one of the other reagent containers becomes depleted before the R1 reagent is depleted.",
      "root_cause_description": "Other",
      "action": "Customers were notified by certified mail on or about May 12, 2003.  Operators were given a workaround (assure R1 has the lower number of tests remaining before using the analyzer) until new software is supplied.",
      "product_quantity": "478",
      "distribution_pattern": "United States",
      "openfda": {}
    }
  ]
}