{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Los Altos",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72810",
      "recalling_firm": "RenovoRx, Inc.",
      "address_1": "4546 El Camino Real Ste 282",
      "address_2": "N/A",
      "postal_code": "94022-1068",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of : CA  and  FL.",
      "recall_number": "Z-0565-2016",
      "product_description": "RenovoCath RC 120;  Temporary Intravascular Occluding Catheter  Model number: MMRC120-DB-1111;  Rx only.    Cardiovascular: The RenovoCath RC120 Catheter is intended for the isolation of blood flow and delivery of fluids, including diagnostic and/or therapeutic agents, to selected sites in the peripheral vascular system.",
      "product_quantity": "11 units",
      "reason_for_recall": "Incorrect version of Instructions for Use were shipped to two US customers.",
      "recall_initiation_date": "20151125",
      "center_classification_date": "20151231",
      "termination_date": "20160229",
      "report_date": "20160106",
      "code_info": "Model number: MMRC120-DB-1111;  Lot number: B2456974A; Expiry 2016-07.  Lot B2457150A - all 72 units were either used or returned prior to initiation of recall."
    }
  ]
}