{
  "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-1910-2026",
      "product_description": "Arrow Echogenic Introducer Needle REF ASK-04001-BWK2  UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347    This device is intended for injection or aspiration of fluids. The needle protection device  covers the needle after use to help prevent needle sticks.",
      "product_quantity": "85",
      "reason_for_recall": "Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured",
      "recall_initiation_date": "20260311",
      "center_classification_date": "20260422",
      "report_date": "20260429",
      "code_info": "Product code: ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347 Batch Number: 33F25J0347",
      "more_code_info": ""
    }
  ]
}