{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "36040",
      "product_res_number": "Z-0331-05",
      "event_date_initiated": "2004-11-12",
      "event_date_posted": "2004-12-21",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-02-21",
      "res_event_number": "30433",
      "product_code": "LNO",
      "k_numbers": [
        "K910332"
      ],
      "product_description": "18 French Ross Flexiflo Over the Guidewire Gastrostomy Kit with T-Fasteners for Endoscopic Removal (list # 00238).",
      "code_info": "Lots: 02581GZOO, 11884GZ00, 17159GZ00.",
      "firm_fei_number": "1527460",
      "recalling_firm": "Abbott Laboratories",
      "address_1": "6550 Singletree Dr",
      "city": "Columbus",
      "state": "OH",
      "postal_code": "43229-1119",
      "additional_info_contact": "Randal P. McKay\n614-624-3688",
      "reason_for_recall": "Gastrostomy and Jejunostomy primary placement kits which may contain components that may not have been adequately sterilized, were distributed.",
      "root_cause_description": "Other",
      "action": "The recalling firm notified customers by letter, dated 11/12/04.",
      "product_quantity": "739 gastrostomy  kits.",
      "distribution_pattern": "The product was distributed throughout the United States and to foreign consignees located in Australia, Korea, Thailand, Venezuela, and Puerto Rico.",
      "openfda": {}
    }
  ]
}