{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Reading",
      "address_1": "2400 Bernville Rd",
      "reason_for_recall": "Arrow AGB+ Multi-Lumen CVC Kit - lidstock incorrectly states within CDC-45703-1A a catheter 20cm in length. The banner card correctly states the product is CDC-42703-1A with a catheter 16cm in length",
      "address_2": "",
      "product_quantity": "745 eaches",
      "code_info": "Lot Number: 13F18L0759",
      "center_classification_date": "20191024",
      "distribution_pattern": "US Nationwide distribution.",
      "state": "PA",
      "product_description": "Arrow AGB+ Multi-Lumen CVC Kit-catheter permits venous access to central circulation by way of subclavian, jugular, and femoral veins  Product Code: CDC-42703-1A - Product Usage: The ARROWg+ard Blue PLUS catheter permits venous access to central circulation by way of subclavian, jugular, and femoral veins. The ARROWg+ard technology is intended to provide protection against catheter-related bloodstream infections (CRBSIs). It is not intended to be used as a treatment for existing infections nor is it indicated for long-term use (> 30 days). Clinical effectiveness of the ARROWg+ard Blue PLUS¿ catheter in preventing CRBSIs compared to the original ARROWg+ard Blue¿ catheter has not been studied.",
      "report_date": "20191030",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-0192-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83456",
      "termination_date": "20201110",
      "more_code_info": "",
      "recall_initiation_date": "20190718",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}