{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Galway",
      "state": "N/A",
      "country": "Ireland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87175",
      "recalling_firm": "Natus Manufacturing Limited",
      "address_1": "Ida Business Park",
      "address_2": "Glenbrack Road",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the state of NY.",
      "recall_number": "Z-1143-2021",
      "product_description": "Ref: NT821731C, Natus EDS 3 CSF External Drainage System - Product Usage:  indicated for draining cerebrospinal fluid (CFS) from the cerebral ventricles or the lumbar subarachnoid space as a means of reducing intracranial pressure and CSF volume when the insertion of a permanent, internal shunt is not indicated.",
      "product_quantity": "7 units",
      "reason_for_recall": "The external drainage system failed to meet Pyrogen test requirements for devices contacting cerebrospinal fluid of 2.15 endotoxins.",
      "recall_initiation_date": "20210112",
      "center_classification_date": "20210222",
      "termination_date": "20221108",
      "report_date": "20210303",
      "code_info": "Lot # 118000422298"
    }
  ]
}