{
  "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": "70175",
      "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": "Nationwide",
      "recall_number": "Z-1082-2015",
      "product_description": "ARROWg+ard Blue PLUS Pressure Injectable Two-Lumen CVC Kit. The Multiple-Lumen Catheter permits venous access to the central circulation by way of the femoral jugular, or subclavian veins.",
      "product_quantity": "1195",
      "reason_for_recall": "Foreign material found within the kits. The foreign material, white or black particles and/or thread, is  visible and can beidentified by the user.",
      "recall_initiation_date": "20150102",
      "center_classification_date": "20150210",
      "termination_date": "20161025",
      "report_date": "20150218",
      "code_info": "product number CDC-42802-P1A, lot  number 23F14A0063"
    }
  ]
}