{
  "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": [
    {
      "status": "Terminated",
      "city": "Fremont",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69669",
      "recalling_firm": "Stryker Neurovascular",
      "address_1": "47900 Bayside Pkwy",
      "address_2": "N/A",
      "postal_code": "94538-6515",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of: VA, NH, OH and TX.",
      "recall_number": "Z-0482-2015",
      "product_description": "Gateway OTW 2.75mm x 9mm;    The Gateway PTA balloon catheter is indicated for balloon dilation of the stenotic portion of intracranial arteries for the purpose of improving intracranial perfusion.",
      "product_quantity": "1 unit",
      "reason_for_recall": "Units of GDC 360 coils, Target coil and Gateway PTA Balloon Catheter were shipped to US customers beyond the expiration date.",
      "recall_initiation_date": "20141022",
      "center_classification_date": "20141128",
      "termination_date": "20150212",
      "report_date": "20141210",
      "code_info": "Model M00320072209270, Lot number: 12693091;  Exp. Jun 2012."
    }
  ]
}