{
  "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-0830-2018",
      "product_description": "Mallinckrodt Institute Percutaneous  Gastrostomy Set     Product Usage:  Intended for the percutaneous placement of a catheter for gastroenteric feeding",
      "product_quantity": "615",
      "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-1400 -MKOT-A  Lot numbers: 6869315  6908857  7034661  7106057  7193431  7252317  7635697  7744001  7811587  8025220  8076495"
    }
  ]
}