{
  "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": "Menlo Park",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64625",
      "recalling_firm": "Acclarent, Inc.",
      "address_1": "1525-B O'Brien Dr",
      "address_2": "N/A",
      "postal_code": "94025-1463",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) and the countries of  Belgium, Canada, and Saudi Arabia.",
      "recall_number": "Z-1864-2013",
      "product_description": "Inspira AIR Balloon Dilation system.  Size 12 x 40 mm, Syringe volume 12 cc.    Dilation of airway tree.",
      "product_quantity": "1217",
      "reason_for_recall": "Labeling correction for all sizes of the Inspira AIR Balloon Dilation System to include additional language and warnings as well as to clarify some instructional steps.",
      "recall_initiation_date": "20130111",
      "center_classification_date": "20130801",
      "termination_date": "20131025",
      "report_date": "20130807",
      "code_info": "Product code: BC1240A;  All lots manufactured after March 1, 2011",
      "more_code_info": ""
    }
  ]
}