{
  "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,
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    }
  },
  "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-0479-2015",
      "product_description": "GDC-10 360 10mm x 30cm SR ;    GDC 360¿ Detachable Coils are intended for embolization of those intracranial aneurysms that- because of their morphology, their location, or the patient 's  general medical condition - are considered by the  treating neurosurgical team to be    a) very high risk for management by traditional operative techniques, or b) inoperable",
      "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 M0033461030SRO, Lot number: 13239506;  Exp. Jan 2013."
    }
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}