{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Indianapolis",
      "address_1": "9115 Hague Rd",
      "reason_for_recall": "Complaints have been received concerning questionable results on analyzers due to customers utilizing 13 sample tubes without tube adapters.",
      "address_2": "",
      "product_quantity": "",
      "code_info": "None",
      "center_classification_date": "20180328",
      "distribution_pattern": "US Nationwide",
      "state": "IN",
      "product_description": "c6000, Chemistry (Photometric, Discrete), for clinical use. - cobas e 601 module: Immunoassay Analyzer, Catalog Numbers: 04745922001, 05036348001, 05860652001, 04745922692, 05036348001 & 05036348692",
      "report_date": "20180404",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Roche Diagnostics Corporation",
      "recall_number": "Z-1268-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79074",
      "termination_date": "20190409",
      "more_code_info": "",
      "recall_initiation_date": "20171218",
      "postal_code": "46256-1025",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}