{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Bloomington",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79192",
      "recalling_firm": "Cook Inc.",
      "address_1": "750 N Daniels Way",
      "address_2": "N/A",
      "postal_code": "47404-9120",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-0832-2018",
      "product_description": "Wills-Oglesby Percutaneous Gastrostomy Set  Product Usage:  Intended for the percutaneous placement of a catheter for gastroenteric feeding",
      "product_quantity": "Quantities co-mingled into line 1",
      "reason_for_recall": "Cook has identified that the affected lots may contain wire guides that were loaded backwards into the wire guide holder.",
      "recall_initiation_date": "20171019",
      "center_classification_date": "20180301",
      "termination_date": "20190416",
      "report_date": "20180307",
      "code_info": "WOGS-1200  Lot numbers: 6709866  7092684  7225148  7315120  7360624  7428977  7464543  7523606  7580747  7580749  7852593  7897499  7981709  8032023"
    }
  ]
}