{
  "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-2336-2017",
      "product_description": "Arrow Multi-Lumen CVC Kit  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": "The Arrow CVC is indicated to provide short-term (<30 days) central venous access for treatment of diseases or conditions requiring central venous access including, but not limited to:  -multiple infusions of fluids, medications, or chemotherapy  -infusion of fluids that are hypertonic, hyperosmolar, or have divergent pH values  -frequent blood sampling or blood/blood components infusions  -infusion of incompatible medications  -central venous pressure monitoring  lack of usable peripheral IV sites  -replacement of multiple peripheral sites for IV access",
      "recall_initiation_date": "20170509",
      "center_classification_date": "20170612",
      "termination_date": "20180917",
      "report_date": "20170621",
      "code_info": "Material number: CDC-12703-1A, CDC-12802-1A, CDC-15703-1A, CDC-15703-B1A, CDC-15802-1A,   Device Listing E426708"
    }
  ]
}