{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Reading",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70436",
      "recalling_firm": "Arrow International Inc",
      "address_1": "2400 Bernville Road",
      "address_2": "N/A",
      "postal_code": "19605",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and Internationally to Belgium",
      "recall_number": "Z-1233-2015",
      "product_description": "ARROW FiberOptix Intra-Aortic Balloon Catheter Kit, 40 cc 7.5 Fr  Product Code: IAB-05840-LWS  The Arrow IAB is utilized for intra-aortic balloon counter-pulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood supply to the heart muscle and decreases work of the left ventricle",
      "product_quantity": "165 units",
      "reason_for_recall": "Outer package product label incorrectly identifies the product as  FiberOptix Flex IAB 7.5Fr  rather than the correct \u001cFiberOptix IAB 8Fr",
      "recall_initiation_date": "20150205",
      "center_classification_date": "20150302",
      "termination_date": "20161026",
      "report_date": "20150311",
      "code_info": "Lot Number: 18F14M0001"
    }
  ]
}