{
  "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,
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    }
  },
  "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-1912-2026",
      "product_description": "PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3  UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352    The Arrow¿ percutaneous sheath introducer permits venous access and catheter  introduction to the central circulation.",
      "product_quantity": "115",
      "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-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 Batch Number: 33F25K0130",
      "more_code_info": ""
    }
  ]
}