{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Morrisville",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98618",
      "recalling_firm": "ARROW INTERNATIONAL, LLC",
      "address_1": "3015 Carrington Mill Blvd",
      "address_2": "N/A",
      "postal_code": "27560-5437",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA, and VA.",
      "recall_number": "Z-1917-2026",
      "product_description": "Arrowg+ard Blue¿ MAC\" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-21142-DMC  UDI code: (01)10801902218930(17)270630(11)251211(10)33F25M0671      The MAC Multi-Lumen Central Venous Access Device with Arrowg+ard Blue technology  permits short-term (<30 days) venous access and catheter introduction to the  central circulation. It may be inserted into the jugular, subclavian, or femoral veins.  The Arrowg+ard technology is intended to help provide protection against catheterrelated  infections. Clinical data have not been collected that demonstrate the use of the  Arrowg+ard antimicrobial surface in decreasing catheter-related infections for this device.  It is not intended to be used as a treatment for existing infections, nor is it indicated for  long-term use.",
      "product_quantity": "95",
      "reason_for_recall": "Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured",
      "recall_initiation_date": "20260311",
      "center_classification_date": "20260422",
      "report_date": "20260429",
      "code_info": "Product Code: ASK-21142-DMC UDI code: (01)10801902218930(17)270630(11)251211(10)33F25M0671 Batch Number: 33F25M0671",
      "more_code_info": ""
    }
  ]
}