{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Ocala",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71263",
      "recalling_firm": "American Catheter Corp",
      "address_1": "13047 S Highway 475",
      "address_2": "N/A",
      "postal_code": "34480-8503",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Distributed in the states of AL, AK, CA, CO, FL, GA, HI, IL, KS, LA, MI, MO, MT, NJ, OH, OK, SC, TN, TX, WA, and WI.",
      "recall_number": "Z-2191-2015",
      "product_description": "American Catheter / Cholangiogram Catheter 9100 Series.",
      "product_quantity": "890 devices.",
      "reason_for_recall": "Catheters were not sealed before sterilization. and was not detected through subsequent acceptance activities, product release and distribution.",
      "recall_initiation_date": "20150317",
      "center_classification_date": "20150722",
      "termination_date": "20161214",
      "report_date": "20150729",
      "code_info": "Product Number is 9100, Lot # 14101601."
    }
  ]
}