{
  "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": [
    {
      "status": "Terminated",
      "city": "Murray",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72018",
      "recalling_firm": "Clinical Innovations, LLC",
      "address_1": "747 W 4170 S",
      "address_2": "N/A",
      "postal_code": "84123-1364",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "Nationwide to MS, MD, TN, NC, IN, FL, AL, and LA, and to France.",
      "recall_number": "Z-0123-2016",
      "product_description": "The Ebb Complete Tamponade System, model #CTS-1000 and Code #OQY.  Intended for use in providing temporary control or reduction of postpartum uterine bleeding.",
      "product_quantity": "827 units",
      "reason_for_recall": "Clinical Innovations, LLC is voluntarily recalling the Ebb Complete Tamponade System (CTS-1000) Lot Number 1214-F-403.) to address the potential for a balloon leak which may affect the ability to deliver therapy, when needed.",
      "recall_initiation_date": "20150105",
      "center_classification_date": "20151015",
      "termination_date": "20160421",
      "report_date": "20151021",
      "code_info": "Manufacturing lot 1214-F-403 and 1214-V-424"
    }
  ]
}