{
  "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": "62774",
      "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": "Other",
      "distribution_pattern": "Nationwide distribution: USA",
      "recall_number": "Z-2327-2012",
      "product_description": "Bard Foley procedural trays packaged in breather bags.  The product is packaged ten units in each shipper box, and are sold sterile for single use.    Used to catheterize patients. The finished trays are sold in Tyvek breather bags.",
      "product_quantity": "56,694 units",
      "reason_for_recall": "Incomplete seal on sterile packages of product.",
      "recall_initiation_date": "20120629",
      "center_classification_date": "20120907",
      "termination_date": "20130207",
      "report_date": "20120919",
      "code_info": "Catalog No. 300316A (Lot Nos. - NGVJ1108, NGVJ1712, NGVJ1713, NGVJ1105, NGVJ1714)  Catalog No. 898316 (Lot Nos. NGVJ1614, NGVJ1615, NGVJ1616, NGVJ1617)  Catalog No. 897414 (Lot No.  NGVJ1705)  Catalog No. 907618 (Lot No.  NGVJ1757)  Catalog No. 907600 (Lot No.  NGVJ1764)"
    }
  ]
}