{
  "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": "88499",
      "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": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-2529-2021",
      "product_description": "Catalog A800061, SureStep\" Foley Tray, Bard LubricathTM Foley Catheter Tray",
      "product_quantity": "2660 units",
      "reason_for_recall": "There is potential for packaging defects that may impact the sterile barrier.",
      "recall_initiation_date": "20210805",
      "center_classification_date": "20210923",
      "report_date": "20210929",
      "code_info": "Catalog A800061, Lot NGFR3658, UDI (01)00801741104848(17)251228(10)",
      "more_code_info": ""
    }
  ]
}