{
  "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-1916-2026",
      "product_description": "MAC\" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-11142-LC2  UDI code: (01)10801902206807(17)270531(11)251211(10)33F25M0670    The MAC Multi-Lumen Central Venous Access Device permits short-term (<30 days) venous  access and catheter introduction to the central circulation.",
      "product_quantity": "90",
      "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-11142-LC2 UDI code: (01)10801902206807(17)270531(11)251211(10)33F25M0670 Batch Number: 33F25M0670",
      "more_code_info": ""
    }
  ]
}