{
  "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": "Covington",
      "address_1": "8195 Industrial Blvd NE",
      "reason_for_recall": "The product contained a latex catheter instead of a silicone catheter.",
      "address_2": "",
      "product_quantity": "2690 units",
      "code_info": "NGAQ4149",
      "center_classification_date": "20170109",
      "distribution_pattern": "US Distribution to the states of : CA, CT, FL, GA, IL, IN, KS, KY, MD, MA, MI, NE, NV, NJ, NM, NY, OR, SC, TN, TX, UT, VA, WA",
      "state": "GA",
      "product_description": "SURESTEP Tray, BARDEX I.C. COMPLETE CARE, Urine Meter, Temperature STATLOCK Stabilization Device",
      "report_date": "20170118",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "C.R. Bard, Inc.",
      "recall_number": "Z-0967-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75952",
      "termination_date": "20211005",
      "more_code_info": "",
      "recall_initiation_date": "20160711",
      "postal_code": "30014-1497",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}