{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85430",
      "recalling_firm": "Kentec Medical, Inc",
      "address_1": "17871 Fitch",
      "address_2": "",
      "postal_code": "92614-6001",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: CA, IA, and VA",
      "recall_number": "Z-2516-2020",
      "product_description": "Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes. Sterile and single use only. Catalog number ENF-60P-50 (6 fr. 50 cm ENFit Enteral Feeding Tube).",
      "product_quantity": "710",
      "reason_for_recall": "Feeding tube plastic tethered closure cap may possibly fracture or break. Possible health hazards:  (1) Enteral feeding and medication administration could be possibly delayed, until replacement tube is placed into patient  (2) Patient could be unnecessarily overexposed to radiation if multiple x-rays are needed to confirm placement of a new tube, if x-ray is used as the placement confirmation method.",
      "recall_initiation_date": "20200117",
      "center_classification_date": "20200706",
      "termination_date": "20221021",
      "report_date": "20200715",
      "code_info": "Lot Number: KS1706021",
      "more_code_info": ""
    }
  ]
}