{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Covington",
      "address_1": "8195 Industrial Blvd NE",
      "reason_for_recall": "The possibility exists that use of the Uros Automated Urine Output and Temperature Monitor may lead to the loss of urine output measurement data and/or urine output measurement inaccuracies resulting in an impact on clinical treatment decisions.",
      "address_2": "",
      "product_quantity": "2 units",
      "code_info": "Catalog/PC #BK10001M",
      "center_classification_date": "20180129",
      "distribution_pattern": "US Distribution to the state of: FL",
      "state": "GA",
      "product_description": "BARD UROS AUTOMATED URINE OUPTUT AND TEMPERATURE MONITOR, MODEL BK10001M     The Uros(TM) Automated Urine Output and Temperature Monitor is indicated to monitor urine output and core bladder temperature.",
      "report_date": "20180207",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "C.R. Bard, Inc.",
      "recall_number": "Z-0488-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "78231",
      "termination_date": "20210707",
      "more_code_info": "",
      "recall_initiation_date": "20170929",
      "postal_code": "30014-1497",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}