{
  "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": "5,744 units",
      "code_info": "Lot No.    206843112  206854300  206875578  206923218  206951123  206962974  206986677  207167084  207246210  207312741  207441171  207466011  207466012  207560684  207632971  207659577  207716835  207716836  207766493  207900255  207945036  207983301  208008802",
      "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, Catalog No. 46914.    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-1921-2014",
      "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"
    }
  ]
}