{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Goleta",
      "address_1": "125 Cremona Dr",
      "reason_for_recall": "Medtronic Neurosurgery is recalling the Medtronic Duet External Drainage and Monitoring Systems because the patient line tubing in the Duet External Drainage and Monitoring Systems may become disconnected from the patient line stopcock.",
      "address_2": "",
      "product_quantity": "1,187 units",
      "code_info": "Lot No.    206843114  206854302  206923345  207167085  207246211  207466015  207565607  207716842  207766492  208031202",
      "center_classification_date": "20140627",
      "distribution_pattern": "Worldwide Distribution -- USA, Australia, Belgium, Canada, Croatia, Cyprus, Denmark, Egypt, Finland, France, Greece, Iran, Israel, Italy, Kuwait, Netherlands, Norway, Poland, Puerto Rico, Romania, Russian Federation, Saudi Arabia, Singapore, South Africa, Switzerland, Turkey, and United Kingdom.",
      "state": "CA",
      "product_description": "Medtronic Duet External Drainage and Monitoring System, SmartSite Injection Sites, Ventricular Catheter, Catalog No. 46916.    Intended to allow drainage and measurement of cerebrospinal fluid (CSF) and other fluids of similar physical character from the ventricles or the lumbar subarachnoid (intrathecal) region.",
      "report_date": "20140709",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Medtronic Neurosurgery",
      "recall_number": "Z-1923-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68503",
      "termination_date": "20150114",
      "more_code_info": "",
      "recall_initiation_date": "20140609",
      "postal_code": "93117-3083",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}