{
  "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": [
    {
      "country": "United States",
      "city": "Buffalo Grove",
      "address_1": "1001 Asbury Dr",
      "reason_for_recall": "Firm is initiating voluntary correction of CORFLO PEG with ENFit. Barb connector (stem) of the adapter may break unexpectedly when exposed to stress.",
      "address_2": "",
      "product_quantity": "8 cases (2 units per case)",
      "code_info": "Catalogue Numbers: 50-6016",
      "center_classification_date": "20170524",
      "distribution_pattern": "Worldwide distribution in the states of NH, VT, CA and the countries of UK, Ireland, France, Austria, Norway, Sweden, New Zealand",
      "state": "IL",
      "product_description": "CORFLO PEG Kit, Pull 16FR.      Product Usage:  CORFLO PEG Tubes are intended for delivery of enteral nutrition, water and medications into the stomach. The PEG adapter is the connection point between the tubing and the feeding set/syringe. The adapter is designed as a replaceable component.",
      "report_date": "20170531",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "CORPAK MedSystems, Inc.",
      "recall_number": "Z-2163-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76465",
      "termination_date": "20190805",
      "more_code_info": "",
      "recall_initiation_date": "20170203",
      "postal_code": "60089-4528",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}