{
  "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": [
    {
      "country": "United States",
      "city": "Bloomington",
      "address_1": "750 N Daniels Way",
      "reason_for_recall": "This lot of VentriClear failed endotoxin testing.  Potential adverse events include immune responses ranging from non-specific febrile reaction to life-threatening systemic inflammatory response syndrome (SIRS).",
      "address_2": "",
      "product_quantity": "250",
      "code_info": "lot 8639185",
      "center_classification_date": "20180811",
      "distribution_pattern": "One distributor in Indiana; product was not further distributed to end users.",
      "state": "IN",
      "product_description": "VentriClear Ventricular Drainage Catheter Set, Cat. No. N-VVDC-01-ABRM    Product Usage:  The VentriClear Ventricular Drainage Catheter Set has been designed for obtaining access to a ventricular cavity of the brain for short-term use to externally drain fluid for the purpose of relieving elevated intracranial pressure or fluid volume.",
      "report_date": "20180822",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Cook Inc.",
      "recall_number": "Z-2791-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "80492",
      "termination_date": "20190411",
      "more_code_info": "",
      "recall_initiation_date": "20180531",
      "postal_code": "47404-9120",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}