{
  "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": "3,026 units",
      "code_info": "Lot No.    206923217  207096627  207096630  207187691  207224897  207269986  207466017  207565424  207565425  207659575  207659576  207739874  207875274  207945037  207982847",
      "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, Interlink Injection Sites, Catalog No. 46913.    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-1920-2014",
      "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"
    }
  ]
}