{
  "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": "82394",
      "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": "Letter",
      "distribution_pattern": "Distributed to accounts in AL  AZ  CA  CT  FL  HI  IA  IL  IN  KY  LA  MA  MD  ME  MI  MN  MO  NC  NH  NJ  NY  OH  OR  PA  PR  SC  TN  TX  VA  WA  WI",
      "recall_number": "Z-1249-2019",
      "product_description": "cobas e 801 immunoassay analyzer",
      "product_quantity": "149",
      "reason_for_recall": "The firm has confirmed complaints regarding signal drops on the cobas e 801 module after a ProCell II M bottle changeover, which may lead to incorrect medical decisions with respect to diagnostics and patient treatment.",
      "recall_initiation_date": "20190315",
      "center_classification_date": "20190502",
      "termination_date": "20200423",
      "report_date": "20190508",
      "code_info": "All units may experience this issue."
    }
  ]
}