{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Covington",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92082",
      "recalling_firm": "C.R. Bard Inc",
      "address_1": "8195 Industrial Blvd Ne",
      "address_2": "",
      "postal_code": "30014-1497",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide",
      "recall_number": "Z-1700-2023",
      "product_description": "Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G",
      "product_quantity": "5760 devices",
      "reason_for_recall": "Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that could impact product sterility.",
      "recall_initiation_date": "20230420",
      "center_classification_date": "20230608",
      "report_date": "20230614",
      "code_info": "a) REF 52810G, UDI/DI 00801741136870, Lot Numbers:  JUGW1445",
      "more_code_info": ""
    }
  ]
}