{
  "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": "Potential breach of the sterile barrier packaging.",
      "address_2": "",
      "product_quantity": "14,310 each",
      "code_info": "Lot Number 73600023",
      "center_classification_date": "20150814",
      "distribution_pattern": "Nationwide Distribution-including  AL, AZ, AR, CA, CO, CT, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NV, NH, NJ, NY, NC, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WV, WI AND DC.",
      "state": "GA",
      "product_description": "Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6\"), 10 Fr, (30/box), Product Code 51610.    Intermittent catheter.",
      "report_date": "20150826",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "C.R. Bard, Inc.",
      "recall_number": "Z-2384-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71722",
      "termination_date": "20170721",
      "more_code_info": "",
      "recall_initiation_date": "20150707",
      "postal_code": "30014-1497",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}