{
  "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": "77232",
      "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": "Worldwide Distribution - US (nationwide) and Canada",
      "recall_number": "Z-2334-2017",
      "product_description": "1) ARROWg+ard Blue You-Blend Two-Lumen Hemodialysis Catheterization Kit for High Volume Infusions  The large-bore two-lumen catheter permits venous access to the central circulation for rapid fluid administration, temporary or acute hemodialysis, apheresis and hemofiltration. It may be inserted into the jugular, subclavia, or femoral veins    Catheter, hemodialysis non-implanted",
      "product_quantity": "27,485 units distributed in the U.S., 4,371 units distributed internationally",
      "reason_for_recall": "Arrow International is recalling the affected product because the packaging may not be completely sealed, which may compromise sterility.",
      "recall_initiation_date": "20170509",
      "center_classification_date": "20170612",
      "termination_date": "20180917",
      "report_date": "20170621",
      "code_info": "Material number: CDA-22122-U1A, CDC-22141-1A CDC-26142-1A   Device Listing D025726"
    }
  ]
}