{
  "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": [
    {
      "status": "Terminated",
      "city": "Mountain View",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70847",
      "recalling_firm": "Hansen Medical Inc",
      "address_1": "800 E Middlefield Rd",
      "address_2": "N/A",
      "postal_code": "94043-4030",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "Worldwide Distribution - US Distribution and the countries of : Saudi Arabia, Australia, France, Italy, Germany, and United Kingdom.",
      "recall_number": "Z-1449-2015",
      "product_description": "Magellan Robotic System; Model No(s). 11132 and 11139.  A steerable catheter control system used at clinical sites.",
      "product_quantity": "19 total installed systems",
      "reason_for_recall": "Based on investigation of two complaint incidents, all Hansen Medical Magellan Robotic System (Model No. 11132 and 11139) may experience an unexpected event during a retraction operation of catheter.  Retraction of catheter may not stop when equipment button is released.",
      "recall_initiation_date": "20150318",
      "center_classification_date": "20150415",
      "termination_date": "20150923",
      "report_date": "20150422",
      "code_info": "All serial numbers."
    }
  ]
}