{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Princeton",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96672",
      "recalling_firm": "Integra LifeSciences Corp. (NeuroSciences)",
      "address_1": "1100 Campus Rd",
      "address_2": "N/A",
      "postal_code": "08540-6650",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of TX, MT, AL & OK.",
      "recall_number": "Z-1724-2025",
      "product_description": "INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK. Airway balloon dilation catheter.",
      "product_quantity": "6 units",
      "reason_for_recall": "Incorrect product packaged in INSPIRA AIR Balloon Dilation System carton.",
      "recall_initiation_date": "20250404",
      "center_classification_date": "20250506",
      "report_date": "20250514",
      "code_info": "Model No. BC1040AZ; UDI: 20705031063157; Lot No. 240716A-PC.",
      "more_code_info": ""
    }
  ]
}