{
  "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": "2026-04-15",
    "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": "77671",
      "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": "nationwide",
      "recall_number": "Z-2800-2017",
      "product_description": "Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 20,   Trevo Pro 18 Microcatheter, AXS Catalyst 060x132CM - US, UPN M0033PK42022001",
      "product_quantity": "63 packs",
      "reason_for_recall": "Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs were  manufactured using a carton sleeve where the pre-printed contents on the back of the sleeve did not match the physical contents of the pack.",
      "recall_initiation_date": "20170626",
      "center_classification_date": "20170729",
      "termination_date": "20210329",
      "report_date": "20170809",
      "code_info": "Lot Numbers: QPC30107530, QPC30107745, QPC30107814, QPC30110247"
    }
  ]
}