{
  "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": "70137",
      "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": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and the countries of : Canada, Finland, Estonia, Belgium, Ireland, Sweden, France, Switzerland, Spain, Netherlands, Middle East, Scotland, Germany and Wales.",
      "recall_number": "Z-1014-2015",
      "product_description": "Ebb Complete Tamponade System, BD-OTS Obstetric Catheter, REF CTS-1000, Rx Only, Sterile EO",
      "product_quantity": "827 units",
      "reason_for_recall": "Potential for a balloon leak in all lots of (CTS-1000) manufactured since August 2014.",
      "recall_initiation_date": "20141230",
      "center_classification_date": "20150127",
      "termination_date": "20151228",
      "report_date": "20150204",
      "code_info": "Lots: 0314-F-566; 0814-F-100; 0814-F-108; 0814-V-068"
    }
  ]
}