{
  "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": "2026-04-01",
    "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": "83525",
      "recalling_firm": "Roche Diagnostics Operations, Inc.",
      "address_1": "9115 Hague Rd",
      "address_2": "N/A",
      "postal_code": "46256-1025",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "State  NY  MT  HI  IN  MD  TX  OH  KS  KY  CA  FL  OR  LA  MO  AK",
      "recall_number": "Z-2476-2019",
      "product_description": "cobas e 601 module (cobas 6000 Modular Series system) Part Number: 04745922001",
      "product_quantity": "1 unit",
      "reason_for_recall": "Quality issue with high pressure solenoid valves may cause inaccurate results.",
      "recall_initiation_date": "20190718",
      "center_classification_date": "20190905",
      "termination_date": "20200615",
      "report_date": "20190911",
      "code_info": "Serial # : 31A1-01"
    }
  ]
}