{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Indianapolis",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76078",
      "recalling_firm": "Roche Diagnostics Corporation",
      "address_1": "9115 Hague Rd",
      "address_2": "N/A",
      "postal_code": "46256-1025",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "TX and WA",
      "recall_number": "Z-1090-2017",
      "product_description": "cobas p 612 pre-analytical system;    Pre-analytical sample handling that includes de-capping, Aliquotting and sorting of samples for analysis.",
      "product_quantity": "5",
      "reason_for_recall": "",
      "recall_initiation_date": "20161227",
      "center_classification_date": "20170124",
      "termination_date": "20170804",
      "report_date": "20170201",
      "code_info": "Serial Number  63004316  63004416  63004516  63002816  63002916"
    }
  ]
}