{
  "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": "Tempe",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73835",
      "recalling_firm": "Stryker Sustainability Solutions",
      "address_1": "1810 W Drake Dr",
      "address_2": "N/A",
      "postal_code": "85283-4327",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution to KY.",
      "recall_number": "Z-1626-2016",
      "product_description": "Launcher Guiding Catheter  Model #LA6EBU30.  Used in the coronary or peripheral vascular system..",
      "product_quantity": "2",
      "reason_for_recall": "Device packaging may not be sealed.",
      "recall_initiation_date": "20160404",
      "center_classification_date": "20160509",
      "termination_date": "20160713",
      "report_date": "20160518",
      "code_info": "Lot #481938U"
    }
  ]
}