{
  "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": "Reading",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70603",
      "recalling_firm": "Arrow International Inc",
      "address_1": "2400 Bernville Rd",
      "address_2": "N/A",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution US nationwide (including AZ, NJ, ME, TX, WA), and Germany.",
      "recall_number": "Z-1259-2015",
      "product_description": "Arrow Intra-Aortic Balloon Catheter Kit Fiberoptix  (IAB),   8 Fr 40 cc  Model: IAB-05840-LWS",
      "product_quantity": "166 units",
      "reason_for_recall": "Potential for a leak between the catheter and the bifurcate which would allow helium to escape to the atmosphere.",
      "recall_initiation_date": "20131108",
      "center_classification_date": "20150310",
      "termination_date": "20150316",
      "report_date": "20150318",
      "code_info": "Lot Number: KF1111796  Exp. Date: 11/30/2013"
    }
  ]
}