{
  "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": "80204",
      "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": "China",
      "recall_number": "Z-3020-2018",
      "product_description": "Wingspan Stent System, Rx Only, Sterile EO, Catalog #: M003WE0250090, M003WE0300090, M003WE0350090, M003WE0400090, M003WE0450090,  M003WE0250150, M003WE0300150, M003WE0350150, M003WE0400150, M003WE0450150,  M003WE0250200, M003WE0300200, M003WE0350200, M003WE0400200, M003WE0450200",
      "product_quantity": "11585",
      "reason_for_recall": "Use-related coating damage on delivery catheter shafts of Wingspan delivery catheters were reported",
      "recall_initiation_date": "20180605",
      "center_classification_date": "20180907",
      "termination_date": "20201130",
      "report_date": "20180919",
      "code_info": "All lots."
    }
  ]
}