{
  "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": "534,972 each",
      "code_info": "Lot Number 53620387, 53621274, 53621279",
      "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 Catheter 14 Fr in the Insertion Supply Kit, Product Code 51614S.    Intermittent catheter.",
      "report_date": "20150826",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "C.R. Bard, Inc.",
      "recall_number": "Z-2388-2015",
      "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"
    }
  ]
}