{
  "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-2335-2017",
      "product_description": "Arrow MAC Two-Lumen Central Venous Access Kit  Introducer Catheter  The Arrow Two-Lumen Central Venous Access device permits venous access and catheter introduction to the central circulation",
      "product_quantity": "27,485 units distributed in 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: CDC-11242-1A  Device Listing D025760"
    }
  ]
}