{
  "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": "62125",
      "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": "USA (nationwide)  AL, AZ, AR, CA, CO, FL, GA, IL, IN, KS, LA, MA, MI, MO, NV, NH, NC, OH, PA, TX, VA, WA, and WI.",
      "recall_number": "Z-1823-2012",
      "product_description": "Arrow International, Inc. 7FR 3-Lumen Arrowg+ard Blue Plus(R) Pressure Injectable Central Venous Catheter - Catalog number CDC-42703-XP1A    The multiple-lumen pressure injectable catheter permits venous access to central circulation and injection of contrast media. The ARROWg+ard(R) antimicrobial surface is intended to provide protection against catheter-related infections.",
      "product_quantity": "1,085",
      "reason_for_recall": "Arrow is recalling the product due to the possibility of voids in the catheter hub which could lead to an interlumen crossover.",
      "recall_initiation_date": "20120607",
      "center_classification_date": "20120619",
      "termination_date": "20140403",
      "report_date": "20120627",
      "code_info": "Lot number RF2033361"
    }
  ]
}