{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Menlo Park",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71232",
      "recalling_firm": "Acclarent, Inc.",
      "address_1": "1525B Obrien Dr",
      "address_2": "N/A",
      "postal_code": "94025-1463",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US in the state of Texas",
      "recall_number": "Z-1740-2015",
      "product_description": "RELIEVA FLEX Sinus Guide Catheter F-70.  Catalog number GC070RF.    Product Usage - Sinus Catheter - Intended to provide a means to access the sinus space for diagnostic and therapeutic procedures.  .",
      "product_quantity": "986",
      "reason_for_recall": "Acclarent determined that one single RELIEVA FLEX Sinus Guide Catheter was distributed past it's expiry date.",
      "recall_initiation_date": "20150428",
      "center_classification_date": "20150609",
      "termination_date": "20150610",
      "report_date": "20150617",
      "code_info": "Catalog number GC070RF, Lot 120709i-cm, Expiry 7/31/2014."
    }
  ]
}