{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Menlo Park",
      "address_1": "4055 Campbell Ave",
      "reason_for_recall": "One lot may not have been properly sealed, resulting in a non-sterile device.",
      "address_2": "",
      "product_quantity": "148 devices",
      "code_info": "Lot number 1404-03;  Expiration: March 31, 2016",
      "center_classification_date": "20140904",
      "distribution_pattern": "Worldwide Distribution -- US (nationwide) and countries of: Hong Kong and Switzerland.",
      "state": "CA",
      "product_description": "iTRACK250A Canaloplasty Microcatheter Kit; Catalogue number: iT-250A; Rx only, sterile.    Indicated for fluid infusion and aspiration during surgery.",
      "report_date": "20140910",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ellex iScience, Inc.",
      "recall_number": "Z-2590-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69021",
      "termination_date": "20141028",
      "more_code_info": "",
      "recall_initiation_date": "20140806",
      "postal_code": "94025-1006",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}