{
  "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": "Covington",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63136",
      "recalling_firm": "C.R. Bard, Inc., Urological Division",
      "address_1": "8195 Industrial Blvd Ne",
      "address_2": "N/A",
      "postal_code": "30014-1497",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide distribution: USA and Puerto Rico",
      "recall_number": "Z-0010-2013",
      "product_description": "8 Fr. Bardex Pediatric All-Silicone Foley Catheter with a 3cc balloon.  The product is packaged individually with 12 units per corrugated case.  The product is sold sterile for single use and is used to provide continuous urinary drainage from the bladder.",
      "product_quantity": "4,032 units",
      "reason_for_recall": "The 8 Fr. Bardex All-Silicone Foley Catheter with 3cc balloon had an incorrect inflation volume (10 ml instead of 5 ml) printed on the valve cap.",
      "recall_initiation_date": "20120907",
      "center_classification_date": "20121004",
      "termination_date": "20130321",
      "report_date": "20121010",
      "code_info": "Catalog # 165808, Lot # NGWA1111"
    }
  ]
}