{
  "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": [
    {
      "country": "United States",
      "city": "Reading",
      "address_1": "2400 Bernville Road",
      "reason_for_recall": "Potential to have an internal leak at the fill port of the stainless steel tip, which may necessitate removal and replacement of  the catheter.",
      "address_2": "",
      "product_quantity": "188 units",
      "code_info": "Lot Numbers:  KF2073734   KS2083999   KF2083869  KF2083921",
      "center_classification_date": "20130405",
      "distribution_pattern": "Worldwide Distribution -- USA, Belgium, Great Britain, Italy, Kazakhstan, Latvia, Russia, Slovenia, Turkey, and South Africa.",
      "state": "PA",
      "product_description": "Arrow International FiberOptix Intra-Aortic Balloon Catheter Kit (IAB) 8 Fr  30 cc;  Product Number: IAB-05830-LWS.    The IAB is utilized for intra-aortic balloon counter-pulsation therapy.",
      "report_date": "20130417",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-1064-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64527",
      "termination_date": "20150602",
      "more_code_info": "",
      "recall_initiation_date": "20121127",
      "postal_code": "19605",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}