{
  "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": [
    {
      "country": "United States",
      "city": "Indianapolis",
      "address_1": "9115 Hague Rd",
      "reason_for_recall": "Alarm flags that have a \"<\" symbol in front of them are not displayed on the cobas infinity Validation screen. This issue affects only customers that are doing manual validation on the cobas infinity Validation screen.",
      "address_2": "",
      "product_quantity": "26 accounts",
      "code_info": "All cobas infinity laboratory solution software versions are affected.",
      "center_classification_date": "20200212",
      "distribution_pattern": "Distributed to customers in AK, AL, CA, GA, HI, IA, IL, KY, MA, MI, MN, MO, MS, MT, NJ, NY, OR, SC, and TN.",
      "state": "IN",
      "product_description": "cobas infinity core, Material No. 7154003001. The device is a calculator/data processing module, for clinical use.",
      "report_date": "20200219",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Roche Diagnostics Operations, Inc.",
      "recall_number": "Z-1158-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84697",
      "termination_date": "20201015",
      "more_code_info": "",
      "recall_initiation_date": "20200107",
      "postal_code": "46256-1025",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}