{
  "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": "The products labeling contains inconsistencies.  In certain instances, the lidstock, banner card and shipper label state that the Spring Wire Guide (SWG) within is .032  rather than the correct SWG size .025 .  For other lots in scope the lidstock correctly states the SWG size .025  however the banner card states the incorrect SWG size .032 .",
      "address_2": "",
      "product_quantity": "3640",
      "code_info": "Lot/Batch Numbers: 13F17E0685  13F17F0562  13F17H0141  13F17K0340  13F18B0119  13R17E0685",
      "center_classification_date": "20181114",
      "distribution_pattern": "US Nationwide distribution in the states of CA, FL, ID, IL, MI, NC, NJ, PA, and WI.",
      "state": "PA",
      "product_description": "Arrow AGB+ Multi-Lumen CVC Kit, 7 Fr., 3 Lumen, 20cm catheter length, .025 inch dia. spring-wire guide, Product Code CDC-45703-B1A - Product Usage: The multiple-lumen catheter permits venous access to the central circulation by the way of the femoral, jugular, or subclavian veins. The ARROWg+ard Blue Plus  antimicrobial catheter is intended to help provide protection against catheter-related infections. It is not intended to be used as a treatment for existing infections nor is it indicated for long-term use.",
      "report_date": "20181121",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-0468-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81242",
      "termination_date": "20200923",
      "more_code_info": "",
      "recall_initiation_date": "20180921",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}