{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93678",
      "recalling_firm": "Stryker, Inc.",
      "address_1": "4870 West 2100 South",
      "address_2": "N/A",
      "postal_code": "84104",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AL, FL, GA, HI, IL, MI, NC, NH, OH, PA, TX, VA.",
      "recall_number": "Z-1084-2024",
      "product_description": "Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm",
      "product_quantity": "11 units",
      "reason_for_recall": "The microcatheter IFU contains an intended use that has not been evaluated by the FDA.",
      "recall_initiation_date": "20231206",
      "center_classification_date": "20240214",
      "report_date": "20240221",
      "code_info": "UDI: (01)00815742002386/Lot Number(s): 0000228865 0000370674"
    }
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}